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