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Синдром кільцевої хромосоми 22

ORPHA:1446· ICD-10 Q93.2· Ring chromosome 22 syndrome

Визначення(English summary)

A rare autosomal anomaly characterized by variable clinical features, most commonly including global developmental delay, hypotonia, growth retardation with microcephaly, intellectual disability with severe speech delay, seizures or abnormal EEG, autistic spectrum disorder and other behavioral characteristics.

Поширеність
<1 / 1 000 000
Вік початку
Infancy, Neonatal