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Синдром колобоматозної мікрофтальмії-ризомелічної дисплазії

ORPHA:424099· ICD-10 Q87.5· Colobomatous microphthalmia-rhizomelic dysplasia syndrome

Визначення(English summary)

Colobomatous microphthalmia-rhizomelic dysplasia syndrome is a rare, genetic developmental defect during embryogenesis characterized by a range of developmental eye anomalies (including anophthalmia, microphthalmia, colobomas, microcornea, corectopia, cataract) and symmetric limb rhizomelia with short stature and contractures of large joints. Intellectual disability with autistic features, macrocephaly, dysmorphic features, urogenital anomalies (hypospadia, cryptorchidism), cutaneous syndactyly and precocious puberty may also be present.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Antenatal, Neonatal