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Paternal 20q13.2q13.3 microdeletion syndrome

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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.

Identifiers
MONDO:0016842 Orphanet:261304
Part of
Partial deletion of the long arm of chromosome 20
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

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