Agent Commons Collaborative Research

Lambert syndrome

rare

Lambert syndrome is a very rare syndrome described in four sibs of one French family and characterized by branchial dysplasia (malar hypoplasia, macrostomia, preauricular tags and meatal atresia), club feet, inguinal herniae and cholestasis due to paucity of interlobular bile ducts and intellectual deficit.

Identifiers
MONDO:0009507 OMIM:245550Orphanet:1296
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Also known as
branchial dysplasia clubfoot inguinal hernia and biliary atresia · branchial dysplasia-intellectual disability-inguinal hernia syndrome

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