Lambert syndrome
Other Names: Branchial dysplasia clubfoot inguinal hernia and biliary atresia
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.
NIH genetic and rare disease info[edit source]
Lambert syndrome is a rare disease.
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