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Review
. 2010 Feb 15;154C(1):146-8.
doi: 10.1002/ajmg.c.30232.

Holoprosencephaly due to numeric chromosome abnormalities

Benjamin D Solomon  1 , Kenneth N Rosenbaum, Jeanne M Meck, Maximilian Muenke
Affiliations
Review

Holoprosencephaly due to numeric chromosome abnormalities

Benjamin D Solomon et al. Am J Med Genet C Semin Med Genet. .

Abstract

Holoprosencephaly (HPE) is the most common malformation of the human forebrain. When a clinician identifies a patient with HPE, a routine chromosome analysis is often the first genetic test sent for laboratory analysis in order to assess for a structural or numerical chromosome anomaly. An abnormality of chromosome number is overall the most frequently identified etiology in a patient with HPE. These abnormalities include trisomy 13, trisomy 18, and triploidy, though several others have been reported. Such chromosome number abnormalities are almost universally fatal early in gestation or in infancy. Clinical features of specific chromosome number abnormalities may be recognized by phenotypic manifestations in addition to the HPE.

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