Monosomy 18p

Monosomy 18p refers to a chromosomal disorder resulting from the deletion of all or part of the short arm of chromosome 18.

Small hand

Disproportionately small hand.


Total: 1

                       


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PMID (PMCID)
14708108
 MALE Adult
Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation.
Babovic-Vuksanovic D, Jenkins SC, Ensenauer R, Newman DC, Jalal SM.
Am J Med Genet A. 2004;124A(3):318-22.
His physical examination is remarkable for only a few dysmorphic findings typically seen in 18p- syndrome (round face, hypertelorism, down-slanted palpebral fissures, temporal narrowing, small hands and feet).