𝔖 Bobbio Scriptorium
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391 Molecular studies in holoprosencephaly

Book ID
122944730
Publisher
Elsevier Science
Year
1991
Tongue
English
Weight
146 KB
Volume
164
Category
Article
ISSN
1097-6868

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Holoprosencephaly (HPE) is a common developmental anomaly of the forebrain and midface in which the cerebral hemispheres fail to separate into distinct left and right halves. HPE is extremely heterogeneous. In addition to teratogenic agents, several genes are implicated in the cause of HPE. Using sa

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## Abstract ECLAMC: Latin American Study of Congenital Malformations examined 4,157,224 births (1967–2000), detecting 370 newborns with suspected holoprosencephaly (HPE): 182 (49.2%) had only craniofacial defects; 99 (26.8%) had defects in other systems; (15.1%) had chromosomal anomalies; 5 (1.4%)