Achard syndrome

MONDO:0007036

A rare genetic syndrome featuring connective tissue abnormalities. Clinical signs include brachycephaly, arachnodactyly, receding mandible and joint laxity at the hands and feet.

Also known as: Achard syndrome, arachnodactyly, receding lower jaw and joint laxity of hands/feet

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

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↑ Hereditary disease (18235) ↑ Syndromic disease (7158)

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

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