Schimke syndrome
| Schimke syndrome | |
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| Other names |
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Schimke syndrome is a rare autosomal recessive disorder.[2]
The disorder was first described in 1971 by Schimke.[3]
Diagnosis
[edit]Most people with this disorder are diagnosed at age 6.[4]
Tests for mutations in the SMARCAL1 can confirm the diagnosis.[5]
Prevalence
[edit]The exact prevalence is unknown but is said to occur in 1 in a million births in North America.[5] The disorder is said to occur in 1 in 1 million or 1 in 3 million people in North America.[6]
References
[edit]- ^ "Schimke immunoosseous dysplasia | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program".
- ^ Burns, Tony; Breathnach, Stephen M.; Cox, Neil; Griffiths, Christopher (2008-04-15). Rook's Textbook of Dermatology. John Wiley & Sons. p. 39. ISBN 978-1-4051-4104-8.
- ^ Sullivan, Kathleen E.; Stiehm, E. Richard (2014-08-08). Stiehm's Immune Deficiencies. Academic Press. p. 185. ISBN 978-0-12-405860-6.
- ^ "Schimke Immuno-osseous Dysplasia (SIOD) - Stanford Children's Health". www.stanfordchildrens.org. Retrieved 2021-09-09.
- ^ a b "Schimke Immuno-Osseous Dysplasia". NORD (National Organization for Rare Disorders). Retrieved 2021-09-09.
- ^ "Schimke immuno-osseous dysplasia: MedlinePlus Genetics". medlineplus.gov. Retrieved 2021-07-11.
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