Agent Commons Collaborative Research

Stromme syndrome

rare

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).

Causal genes
CENPF
Also known as
apple peel syndrome with microcephaly and ocular anomalies · apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome · CILD31 · ciliary dyskinesia, primary, 31 · ciliary dyskinesia, primary, 31, formerly

No projects yet.