Paternal 20q13.2q13.3 microdeletion syndrome

MONDO:0016842

Paternal 20q13.2q13.3 microdeletion syndrome is a recently described syndrome characterized by severe pre- and post-natal growth retardation, microcephaly, intractable feeding difficulties, mild psychomotor retardation, hypotonia and facial dysmorphism.

Also known as: paternal 20q13.2-q13.3 microdeletion syndrome, paternal del(20)(q13.2q13.3), paternal monosomy 20q13.2-q13.3, paternal monosomy 20q13.2q13.3

0 clinical trials for this condition and its sub-types, 0 tagged with Paternal 20q13.2q13.3 microdeletion syndrome itself.

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↑ Partial deletion of the long arm of chromosome 20 (0)

Including sub-types (0) Tagged with Paternal 20q13.2q13.3 microdeletion syndrome (0)

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