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% What Is Stromme Syndrome? Health ConditionsFeaturedBreast CancerIBD MigraineMultiple Sclerosis (MS)Rheumatoid ArthritisType 2 DiabetesSponsored TopicsArticlesAcid RefluxADHDAllergiesAlzheimer&#x27;s &amp; DementiaBipolar DisorderCancerCrohn&#x27;s DiseaseChronic PainCold &amp; FluCOPDDepressionFibromyalgiaHeart DiseaseHigh CholesterolHIVHypertensionIPFOsteoarthritisPsoriasisSkin Disorders and CareSTDsDiscoverWellness TopicsNutritionFitnessSkin CareSexual HealthWomen&#x27;s HealthMental HealthSleepOriginal SeriesFresh Food FastDiagnosis DiariesYou’re Not AlonePresent TenseVideo SeriesYouth in FocusHealthy HarvestNo More SilenceFuture of HealthPlanHealth ChallengesMindful EatingSugar SavvyMove Your BodyGut HealthMood FoodsAlign Your SpineFind CarePrimary CareMental HealthOB-GYNDermatologistsNeurologistsCardiologistsOrthopedistsLifestyle QuizzesWeight ManagementAm I Depressed? A Quiz for TeensAre You a Workaholic?How Well Do You Sleep?Tools &amp; ResourcesHealth NewsFind a DietFind Healthy SnacksDrugs A-ZHealth A-ZConnectFind Your Bezzy CommunityBreast CancerInflammatory Bowel DiseasePsoriatic ArthritisMigraineMultiple SclerosisPsoriasisFollow us on social mediaShopProducts by ConditionInsomniaStress ReliefBack PainNeck PainSleep ApneaHot SleepersAllergiesPain ReliefProduct ReviewsVitamins &amp; SupplementsSleepMental HealthNutritionAt-Home TestingCBDMen’s HealthWomen’s HealthHealth ConditionsDiscoverPlanConnectShopSubscribe <h1>Understanding Stromme Syndrome</h1>Medically reviewed by William C Lloyd III, MD, FACS — By Ashley Marcin on October 19, 2022Stromme syndrome is a rare genetic disorder that affects various areas of a person’s body, including their intestines, eyes, and skull.
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% What Is Stromme Syndrome? Health ConditionsFeaturedBreast CancerIBD MigraineMultiple Sclerosis (MS)Rheumatoid ArthritisType 2 DiabetesSponsored TopicsArticlesAcid RefluxADHDAllergiesAlzheimer's & DementiaBipolar DisorderCancerCrohn's DiseaseChronic PainCold & FluCOPDDepressionFibromyalgiaHeart DiseaseHigh CholesterolHIVHypertensionIPFOsteoarthritisPsoriasisSkin Disorders and CareSTDsDiscoverWellness TopicsNutritionFitnessSkin CareSexual HealthWomen's HealthMental HealthSleepOriginal SeriesFresh Food FastDiagnosis DiariesYou’re Not AlonePresent TenseVideo SeriesYouth in FocusHealthy HarvestNo More SilenceFuture of HealthPlanHealth ChallengesMindful EatingSugar SavvyMove Your BodyGut HealthMood FoodsAlign Your SpineFind CarePrimary CareMental HealthOB-GYNDermatologistsNeurologistsCardiologistsOrthopedistsLifestyle QuizzesWeight ManagementAm I Depressed? A Quiz for TeensAre You a Workaholic?How Well Do You Sleep?Tools & ResourcesHealth NewsFind a DietFind Healthy SnacksDrugs A-ZHealth A-ZConnectFind Your Bezzy CommunityBreast CancerInflammatory Bowel DiseasePsoriatic ArthritisMigraineMultiple SclerosisPsoriasisFollow us on social mediaShopProducts by ConditionInsomniaStress ReliefBack PainNeck PainSleep ApneaHot SleepersAllergiesPain ReliefProduct ReviewsVitamins & SupplementsSleepMental HealthNutritionAt-Home TestingCBDMen’s HealthWomen’s HealthHealth ConditionsDiscoverPlanConnectShopSubscribe

Understanding Stromme Syndrome

Medically reviewed by William C Lloyd III, MD, FACS — By Ashley Marcin on October 19, 2022Stromme syndrome is a rare genetic disorder that affects various areas of a person’s body, including their intestines, eyes, and skull.
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Madison Singh 4 minutes ago
This condition was first discovered in 1993 by a Norwegian pediatrician Petter Strømme. While the s...
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Luna Park 4 minutes ago

What is Stromme syndrome

Stromme syndrome is considered an autosomal recessive congenital ...
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This condition was first discovered in 1993 by a Norwegian pediatrician Petter Strømme. While the syndrome may be fatal for some infants, others may go on to have a typical life expectancy. Here’s what you need to know about Stromme syndrome, what causes it, and what the outlook is for children born with this disorder.
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This condition was first discovered in 1993 by a Norwegian pediatrician Petter Strømme. While the syndrome may be fatal for some infants, others may go on to have a typical life expectancy. Here’s what you need to know about Stromme syndrome, what causes it, and what the outlook is for children born with this disorder.
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Noah Davis 2 minutes ago

What is Stromme syndrome

Stromme syndrome is considered an autosomal recessive congenital ...
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Charlotte Lee 1 minutes ago
Researchers estimate that Stromme syndrome affects fewer than 1 in 1,000,000 births. More specifical...
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<h2>What is Stromme syndrome </h2> Stromme syndrome is considered an autosomal recessive congenital disorder. This means that a person inherits two abnormal genes during conception — one from each parent. In this case, the syndrome is caused by genetic mutations to the person’s CENPF gene.
Aria Nguyen Member
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What is Stromme syndrome

Stromme syndrome is considered an autosomal recessive congenital disorder. This means that a person inherits two abnormal genes during conception — one from each parent. In this case, the syndrome is caused by genetic mutations to the person’s CENPF gene.
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Researchers estimate that Stromme syndrome affects fewer than 1 in 1,000,000 births. More specifical...
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Lily Watson 2 minutes ago

What are the signs and symptoms of Stromme syndrome

Stromme syndrome primarily impacts a p...
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Researchers estimate that Stromme syndrome affects fewer than 1 in 1,000,000 births. More specifically, there have been 13 cases of people with Stromme syndrome discussed in medical literature as of 2019.
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Researchers estimate that Stromme syndrome affects fewer than 1 in 1,000,000 births. More specifically, there have been 13 cases of people with Stromme syndrome discussed in medical literature as of 2019.
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<h2>What are the signs and symptoms of Stromme syndrome </h2> Stromme syndrome primarily impacts a person’s intestines, eyes, and skull. No two people with the syndrome may show exactly the same signs and symptoms, however.Intestinal anomalies: Intestinal anomalies include intestinal atresia (apple peel syndrome), where the small intestine isn’t fully formed and wraps around the blood supply to the colon.Eye anomalies: Eye anomalies include:Epicanthus: Epicanthus is a fold of skin on the eyelid that may cover the inner corner of the eye or eyes.Microcornea: Microcornea is a condition where the cornea (the part that covers the iris and pupil) of the eye or eyes is small.Microphthalmia: Microphthalmia is a condition where one or both eyes are smaller than what is typical.Ptosis: Ptosis is a condition where the upper eyelid may droop over the eye.Sclerocornea: Sclerocornea is a congenital developmental abnormality where the white sclera (white of the eye) extends beyond its normal boundaries onto the clear cornea, reducing some or all of the corneal transparency.Cranial anomalies: Cranial anomalies include microcephaly or a head that’s smaller than average.Cardiac anomalies: Cardiac anomalies include congenital heart defects.Renal anomalies: Renal anomalies include renal (kidney) parenchymal changes and hydronephrosis.Other anomalies: Other anomalies include low platelet count, edema in the lower extremities, hydrocephalus, neuromuscular issues, and cerebellar hypoplasia.
Zoe Mueller Member
access_time 15 minutes ago

What are the signs and symptoms of Stromme syndrome

Stromme syndrome primarily impacts a person’s intestines, eyes, and skull. No two people with the syndrome may show exactly the same signs and symptoms, however.Intestinal anomalies: Intestinal anomalies include intestinal atresia (apple peel syndrome), where the small intestine isn’t fully formed and wraps around the blood supply to the colon.Eye anomalies: Eye anomalies include:Epicanthus: Epicanthus is a fold of skin on the eyelid that may cover the inner corner of the eye or eyes.Microcornea: Microcornea is a condition where the cornea (the part that covers the iris and pupil) of the eye or eyes is small.Microphthalmia: Microphthalmia is a condition where one or both eyes are smaller than what is typical.Ptosis: Ptosis is a condition where the upper eyelid may droop over the eye.Sclerocornea: Sclerocornea is a congenital developmental abnormality where the white sclera (white of the eye) extends beyond its normal boundaries onto the clear cornea, reducing some or all of the corneal transparency.Cranial anomalies: Cranial anomalies include microcephaly or a head that’s smaller than average.Cardiac anomalies: Cardiac anomalies include congenital heart defects.Renal anomalies: Renal anomalies include renal (kidney) parenchymal changes and hydronephrosis.Other anomalies: Other anomalies include low platelet count, edema in the lower extremities, hydrocephalus, neuromuscular issues, and cerebellar hypoplasia.
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Ethan Thomas 7 minutes ago
Physical features associated with Stromme syndrome include:low-set earscleft palatewide mouthwide na...
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While each parent is considered a carrier of the syndrome, neither displays symptoms because their s...
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Physical features associated with Stromme syndrome include:low-set earscleft palatewide mouthwide nasal bridgeextra fingers or toes near the thumb or big toe <h2>What causes Stromme syndrome </h2> Humans have two copies of each gene that they inherit from their parents during conception. Stromme syndrome is caused by mutations to one gene carried by each parent.
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Physical features associated with Stromme syndrome include:low-set earscleft palatewide mouthwide nasal bridgeextra fingers or toes near the thumb or big toe

What causes Stromme syndrome

Humans have two copies of each gene that they inherit from their parents during conception. Stromme syndrome is caused by mutations to one gene carried by each parent.
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William Brown 1 minutes ago
While each parent is considered a carrier of the syndrome, neither displays symptoms because their s...
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While each parent is considered a carrier of the syndrome, neither displays symptoms because their single healthy gene copy overrides the recessive/mutated gene. With Stromme syndrome, the affected infant inherits two copies of the mutated CENPF gene, one from each parent.
Ethan Thomas Member
access_time 7 minutes ago
While each parent is considered a carrier of the syndrome, neither displays symptoms because their single healthy gene copy overrides the recessive/mutated gene. With Stromme syndrome, the affected infant inherits two copies of the mutated CENPF gene, one from each parent.
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Elijah Patel 4 minutes ago
The CENPF gene is responsible for producing a protein called centromere protein F. The disruption to...
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The CENPF gene is responsible for producing a protein called centromere protein F. The disruption to this protein ultimately impacts cell division in the infant’s body during fetal development and results in the various health issues and physical characteristics associated with the syndrome.
Luna Park Member
access_time 40 minutes ago
The CENPF gene is responsible for producing a protein called centromere protein F. The disruption to this protein ultimately impacts cell division in the infant’s body during fetal development and results in the various health issues and physical characteristics associated with the syndrome.
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How is Stromme syndrome diagnosed

A doctor or healthcare professional diagnoses Stromme sy...
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Questions for your doctor

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<h2>How is Stromme syndrome diagnosed </h2> A doctor or healthcare professional diagnoses Stromme syndrome by observing the different symptoms and features of the syndrome at a person’s birth. Genetic testing (through a blood test) can confirm the diagnosis. A doctor may also observe signs of intestinal atresia, microcephaly, eye issues, or other characteristics of Stromme syndrome during pregnancy through a routine ultrasound scan, or they may choose to order additional tests such as a more detailed ultrasound or magnetic resonance imaging (MRI) scan.
Sofia Garcia Member
access_time 27 minutes ago

How is Stromme syndrome diagnosed

A doctor or healthcare professional diagnoses Stromme syndrome by observing the different symptoms and features of the syndrome at a person’s birth. Genetic testing (through a blood test) can confirm the diagnosis. A doctor may also observe signs of intestinal atresia, microcephaly, eye issues, or other characteristics of Stromme syndrome during pregnancy through a routine ultrasound scan, or they may choose to order additional tests such as a more detailed ultrasound or magnetic resonance imaging (MRI) scan.
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Dylan Patel 8 minutes ago

Questions for your doctor

Finding out your child has a rare genetic disorder can be overwhe...
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<h3>Questions for your doctor</h3> Finding out your child has a rare genetic disorder can be overwhelming. A doctor can help answer your questions and point you to others for additional support.
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Questions for your doctor

Finding out your child has a rare genetic disorder can be overwhelming. A doctor can help answer your questions and point you to others for additional support.
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Sophia Chen 7 minutes ago
Questions to get you started:How does my child’s condtion affect the rest of my pregnancy and deli...
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Henry Schmidt 34 minutes ago
Intestinal atresia is common among children with Stromme syndrome. The treatment for this condition ...
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Questions to get you started:How does my child’s condtion affect the rest of my pregnancy and delivery?What testing or observation might be needed after my baby is born?What long-term health issues may my child have?What long-term development issues might my child have?What type of regular medical care/developmental support might my child need?What are our chances of having another child with Stromme syndrome?Where can I find support for families of children with rare disorders? <h2>What is the treatment for Stromme syndrome </h2>There’s no cure for Stromme syndrome. Treatment is targeted at the different symptoms a child has and on improving their quality of life.
Nathan Chen Member
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Questions to get you started:How does my child’s condtion affect the rest of my pregnancy and delivery?What testing or observation might be needed after my baby is born?What long-term health issues may my child have?What long-term development issues might my child have?What type of regular medical care/developmental support might my child need?What are our chances of having another child with Stromme syndrome?Where can I find support for families of children with rare disorders?

What is the treatment for Stromme syndrome

There’s no cure for Stromme syndrome. Treatment is targeted at the different symptoms a child has and on improving their quality of life.
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Intestinal atresia is common among children with Stromme syndrome. The treatment for this condition includes intestinal surgery to address blockages and repair their intestine.
Mia Anderson Member
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Intestinal atresia is common among children with Stromme syndrome. The treatment for this condition includes intestinal surgery to address blockages and repair their intestine.
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Natalie Lopez 12 minutes ago
Surgery may be necessary soon after birth, depending on your child’s condition, and is generally e...
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Surgery may be necessary soon after birth, depending on your child’s condition, and is generally effective. Otherwise, treatment will be individualized to the child and the symptoms they’re experiencing. <h3>Healthcare team</h3> Your child will likely be referred to a children’s hospital where there’s specialized pediatric care.
Luna Park Member
access_time 26 minutes ago
Surgery may be necessary soon after birth, depending on your child’s condition, and is generally effective. Otherwise, treatment will be individualized to the child and the symptoms they’re experiencing.

Healthcare team

Your child will likely be referred to a children’s hospital where there’s specialized pediatric care.
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Evelyn Zhang 24 minutes ago
A number of doctors may consult on your child’s case, including:Perinatologist: Perinatologistspro...
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Aria Nguyen 20 minutes ago
The outlook for people with Stromme syndrome depends on the severity of their symptoms, the body sys...
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A number of doctors may consult on your child’s case, including:Perinatologist: Perinatologistsprovide care before the baby is born.Pediatrician: A pediatricianis responsible for providing overall healthcare for a child.Neurologist: Neurologists provide care for conditions affecting the brain and nervous system.Gastroenterologist: A gastroenterologist treats health conditions of the intestines.Ophthalmologist: An ophthalmologist provides care for conditions of the eyes.Cardiologist: A cardiologist treats conditions affecting the heart.Nephrologist: A nephrologist treats conditions affecting the kidneys.Geneticist: A geneticist is responsible for testing for and diagnosing genetic conditions. <h2>What s the outlook for children with Stromme syndrome </h2>Some babies born with Stromme syndrome may not live long. Others may live to adulthood, including a set of sisters who were reported in 2016 to be living in their twenties.
Andrew Wilson Member
access_time 56 minutes ago
A number of doctors may consult on your child’s case, including:Perinatologist: Perinatologistsprovide care before the baby is born.Pediatrician: A pediatricianis responsible for providing overall healthcare for a child.Neurologist: Neurologists provide care for conditions affecting the brain and nervous system.Gastroenterologist: A gastroenterologist treats health conditions of the intestines.Ophthalmologist: An ophthalmologist provides care for conditions of the eyes.Cardiologist: A cardiologist treats conditions affecting the heart.Nephrologist: A nephrologist treats conditions affecting the kidneys.Geneticist: A geneticist is responsible for testing for and diagnosing genetic conditions.

What s the outlook for children with Stromme syndrome

Some babies born with Stromme syndrome may not live long. Others may live to adulthood, including a set of sisters who were reported in 2016 to be living in their twenties.
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The outlook for people with Stromme syndrome depends on the severity of their symptoms, the body systems involved, and the medical care they receive. Researchers note that some people with Stromme syndrome who do live longer lives may have mild cognitive issues. In other words: The outlook for people with Stromme syndrome is individual.
Emma Wilson Admin
access_time 45 minutes ago
The outlook for people with Stromme syndrome depends on the severity of their symptoms, the body systems involved, and the medical care they receive. Researchers note that some people with Stromme syndrome who do live longer lives may have mild cognitive issues. In other words: The outlook for people with Stromme syndrome is individual.
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Grace Liu 41 minutes ago
Since Stromme syndrome was identified relatively recently, more research is needed to understand the...
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Emma Wilson 19 minutes ago
Instead, it’s a genetically inherited condition. This means it may run in families....
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Since Stromme syndrome was identified relatively recently, more research is needed to understand the outlook for people with this syndrome. <h2>What are the risk factors for Stromme syndrome </h2> There are no environmental risk factors associated with Stromme syndrome.
Andrew Wilson Member
access_time 32 minutes ago
Since Stromme syndrome was identified relatively recently, more research is needed to understand the outlook for people with this syndrome.

What are the risk factors for Stromme syndrome

There are no environmental risk factors associated with Stromme syndrome.
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Instead, it’s a genetically inherited condition. This means it may run in families.
Ethan Thomas Member
access_time 34 minutes ago
Instead, it’s a genetically inherited condition. This means it may run in families.
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Henry Schmidt 19 minutes ago
The abnormality must be passed along when the sperm meets the egg during fertilization. If you or yo...
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The abnormality must be passed along when the sperm meets the egg during fertilization. If you or your partner have a family history of the syndrome, your child may be at higher risk. Two carriers have a 25% chance of passing the syndrome along to their offspring.
Hannah Kim Member
access_time 54 minutes ago
The abnormality must be passed along when the sperm meets the egg during fertilization. If you or your partner have a family history of the syndrome, your child may be at higher risk. Two carriers have a 25% chance of passing the syndrome along to their offspring.
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Ella Rodriguez 36 minutes ago

The takeaway

Stromme syndrome is a rare genetic disorder that has only been recognized for ...
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For any other symptoms, you’ll work with a medical team for an individual approach to help your ch...
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<h2>The takeaway</h2> Stromme syndrome is a rare genetic disorder that has only been recognized for around 30 years. Much of what researchers know is based on available case reports of the few people living with the syndrome. Surgery can effectively address the common intestinal issues associated with the syndrome.
Zoe Mueller Member
access_time 38 minutes ago

The takeaway

Stromme syndrome is a rare genetic disorder that has only been recognized for around 30 years. Much of what researchers know is based on available case reports of the few people living with the syndrome. Surgery can effectively address the common intestinal issues associated with the syndrome.
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For any other symptoms, you’ll work with a medical team for an individual approach to help your ch...
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For any other symptoms, you’ll work with a medical team for an individual approach to help your child thrive. Last medically reviewed on October 19, 2022 <h3>How we vetted this article </h3> SourcesHistoryHealthline has strict sourcing guidelines and relies on peer-reviewed studies, academic research institutions, and medical associations.
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For any other symptoms, you’ll work with a medical team for an individual approach to help your child thrive. Last medically reviewed on October 19, 2022

How we vetted this article

SourcesHistoryHealthline has strict sourcing guidelines and relies on peer-reviewed studies, academic research institutions, and medical associations.
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We avoid using tertiary references. You can learn more about how we ensure our content is accurate a...
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Kevin Wang 36 minutes ago
(2022).
genome.gov/genetics-glossary/Autosomal-Recessive-DisorderCENPF centromere protein F. (20...
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We avoid using tertiary references. You can learn more about how we ensure our content is accurate and current by reading our editorial policy.Autosomal recessive disorder.
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We avoid using tertiary references. You can learn more about how we ensure our content is accurate and current by reading our editorial policy.Autosomal recessive disorder.
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(2022).<br/>genome.gov/genetics-glossary/Autosomal-Recessive-DisorderCENPF centromere protein F. (2022).<br/>ncbi.nlm.nih.gov/gene/1063Dorum BA, et al. (2017).
Madison Singh Member
access_time 88 minutes ago
(2022).
genome.gov/genetics-glossary/Autosomal-Recessive-DisorderCENPF centromere protein F. (2022).
ncbi.nlm.nih.gov/gene/1063Dorum BA, et al. (2017).
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Stromme syndrome: New clinical features.<br/>ncbi.nlm.nih.gov/pmc/articles/PMC5371687/Filges I, et al. (2020). CUGC for Stromme syndrome and CENPF-related disorders.<br/>ncbi.nlm.nih.gov/pmc/articles/PMC6906375/Indiana Government.
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Stromme syndrome: New clinical features.
ncbi.nlm.nih.gov/pmc/articles/PMC5371687/Filges I, et al. (2020). CUGC for Stromme syndrome and CENPF-related disorders.
ncbi.nlm.nih.gov/pmc/articles/PMC6906375/Indiana Government.
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(n.d.). Intestinal atresia.
in.gov/health/files/intestinalatresia.pdfMuula GK....
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(n.d.). Intestinal atresia.<br/>in.gov/health/files/intestinalatresia.pdfMuula GK.
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(n.d.). Intestinal atresia.
in.gov/health/files/intestinalatresia.pdfMuula GK.
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Emma Wilson 36 minutes ago
(2021). Stromme syndrome, causes & symptoms.
jcmedu.org/jcmedu-articles/stromme-syndrome-cau...
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Aria Nguyen 59 minutes ago
A further family of Stromme syndrome carrying CENPF mutation.
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(2021). Stromme syndrome, causes &amp; symptoms.<br/>jcmedu.org/jcmedu-articles/stromme-syndrome-causes--symptoms.pdfOzkinay F, et al. (2017).
William Brown Member
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(2021). Stromme syndrome, causes & symptoms.
jcmedu.org/jcmedu-articles/stromme-syndrome-causes--symptoms.pdfOzkinay F, et al. (2017).
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A further family of Stromme syndrome carrying CENPF mutation.
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(2019). Stromme syndrome; STROMS.
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A further family of Stromme syndrome carrying CENPF mutation.<br/>pubmed.ncbi.nlm.nih.gov/28407396/Petter Stromme. (n.d.).<br/>med.uio.no/klinmed/english/people/aca/pettest/Rasmussen SA.
Chloe Santos Moderator
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A further family of Stromme syndrome carrying CENPF mutation.
pubmed.ncbi.nlm.nih.gov/28407396/Petter Stromme. (n.d.).
med.uio.no/klinmed/english/people/aca/pettest/Rasmussen SA.
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omim.org/entry/243605Rat genome database. (n.d.).
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Gene: Cenpf (centromere protein F) Rattus norvegicus.
rgd.mcw.edu/rgdweb/report/gene/main.html?i...
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Gene: Cenpf (centromere protein F) Rattus norvegicus.<br/>rgd.mcw.edu/rgdweb/report/gene/main.html?id=628667Stromme syndrome. (n.d.).<br/>disorders.eyes.arizona.edu/disorders/strømme-syndromeStromme syndrome.
Lily Watson Moderator
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Gene: Cenpf (centromere protein F) Rattus norvegicus.
rgd.mcw.edu/rgdweb/report/gene/main.html?id=628667Stromme syndrome. (n.d.).
disorders.eyes.arizona.edu/disorders/strømme-syndromeStromme syndrome.
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Harper Kim 13 minutes ago
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(2022).<br/>ncbi.nlm.nih.gov/gtr/conditions/C1855705/Stromme syndrome. (2022).<br/>ncbi.nlm.nih.gov/medgen/340938Our experts continually monitor the health and wellness space, and we update our articles when new information becomes available. Current Version Oct 19, 2022 By Ashley Marcin Edited By Debbie Nurmi Medically Reviewed By William C Lloyd III, MD, FACS Copy Edited By Kristin Hitchcock Share this articleMedically reviewed by William C Lloyd III, MD, FACS — By Ashley Marcin on October 19, 2022 <h3>Read this next</h3>Patients with Rare Diseases Turning to Online Medical Detectives for Help For the last five years, CrowdMed has helped thousands get valuable information about rare and difficult to diagnose conditions.READ MOREWhy Pompe Disease Can Be Mistaken for Other Genetic Diseases Pompe disease shares some similarities with other genetic disorders, but there are tests and analyses that doctors perform to make an accurate…READ MOREWhat Are the Symptoms of Sanfilippo Syndrome?
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(2022).
ncbi.nlm.nih.gov/gtr/conditions/C1855705/Stromme syndrome. (2022).
ncbi.nlm.nih.gov/medgen/340938Our experts continually monitor the health and wellness space, and we update our articles when new information becomes available. Current Version Oct 19, 2022 By Ashley Marcin Edited By Debbie Nurmi Medically Reviewed By William C Lloyd III, MD, FACS Copy Edited By Kristin Hitchcock Share this articleMedically reviewed by William C Lloyd III, MD, FACS — By Ashley Marcin on October 19, 2022

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