X-linked dominant chondrodysplasia, Chassaing-Lacombe type

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X-linked dominant chondrodysplasia, Chassaing-Lacombe type

Synonyms: X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome

X-linked dominant chondrodysplasia Chassaing-Lacombe type is a rare genetic bone disorder characterized by chondrodysplasia intrauterine growth retardation (IUGR) hydrocephaly and facial dysmorphism in the affected males.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.

Reference: Access aggregated data from Orphanet at Orphadata.

Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version September 2023.

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X-linked dominant chondrodysplasia, Chassaing-Lacombe type?

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