Kousseff syndrome

MONDO:0016522

A syndrome characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.

Also known as: sacral meningocele-conotruncal heart defects syndrome, sacral meningocele conotruncal heart defects, sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck

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

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↑ Syndromic disease (7143)

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

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