Lambert syndrome

MONDO:0009507

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.

Also known as: Lambert syndrome, branchial dysplasia-intellectual disability-inguinal hernia syndrome, branchial dysplasia clubfoot inguinal hernia and biliary atresia, branchial dysplasia, clubfoot, inguinal hernia, and biliary atresia

0 clinical trials for this condition and its sub-types, 0 tagged with Lambert syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Lambert syndrome (0)

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