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Stromme syndrome

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Description

Stromme syndrome is an autosomal recessive congenital disorder affecting multiple systems with features of a ciliopathy. Affected individuals typically have some type of intestinal atresia, variable ocular abnormalities, microcephaly, and sometimes involvement of other systems, including renal and cardiac. In some cases, the condition is lethal in early life, whereas other patients show normal survival with or without mild cognitive impairment (summary by Filges et al., 2016).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

21

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Genes

External Links

  • OMIM

    243605

  • Orphanet
  • HPO
  • Medgen

    C1855705

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