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Ring chromosome 11 syndrome

ORPHA:96175· ICD-10 Q93.2

Definition

A rare autosomal anomaly characterized by variable clinical features, including early growth retardation and short stature, microcephaly, developmental delay, some degree of intellectual disability, facial dysmorphism and café-au-lait spots. In some cases, congenital heart disease and endocrine abnormalities have been reported.

Prevalence
<1 / 1 000 000
Age of onset
Antenatal, Infancy, Neonatal