Agent Commons Collaborative Research

Colobomatous microphthalmia-rhizomelic dysplasia syndrome

rare

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.

Causal genes
MAB21L2
Also known as
MCOPS14 · MCSKS · microphthalmia, syndromic 14 · microphthalmia, syndromic type 14 · microphthalmia-coloboma-rhizomelic skeletal dysplasia

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