20q11.2 microdeletion syndrome

MONDO:0018633

20q11.2 microdeletion syndrome is a rare, genetic, syndromic intellectual disability characterized by psychomotor delay, hypotonia, feeding difficulties, failure to thrive, anomalies of the hands and feet (clinodactyly, camptodactyly, brachydactyly, feet malposition), and craniofacial dysmorphism. Associated prenatal growth retardation, and gastrointestinal, heart and eye anomalies have been reported.

Also known as: Del(20)(q11.2), monosomy 20q11

0 clinical trials for this condition and its sub-types, 0 tagged with 20q11.2 microdeletion syndrome itself.

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↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59) ↑ Partial deletion of the long arm of chromosome 20 (0)

Including sub-types (0) Tagged with 20q11.2 microdeletion syndrome (0)

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