X-linked dominant chondrodysplasia, Chassaing-Lacombe type

A rare genetic bone disorder characterized by chondrodysplasia, intrauterine growth retardation (IUGR), hydrocephaly and facial dysmorphism in the affected males.

Also known as: X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, X-linked dominant, chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia

1 clinical trial for this condition and its sub-types.