Holoprosencephaly: A developmental field defect
- 1 October 1989
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 34 (2) , 258-264
- https://doi.org/10.1002/ajmg.1320340228
Abstract
Holoprosencephaly refers to a spectrum of craniofacial malformations including cyclopia, ethmocephaly, cebocephaly, and premaxillary agenesis. Etiologic heterogeneity is well documented. Chromosomal, genetic, and teratogenic factors have been implicated. Recognition of holoprosencephaly as a developmental field defect stresses the importance of close scrutiny of relatives for mild forms such as single median incisor, hyptelorism, bifid uvula, of potuitary deficiency.Keywords
This publication has 42 references indexed in Scilit:
- Holoprosencephaly: Association with interstitial deletion of 2p and review of the cytogenetic literatureAmerican Journal of Medical Genetics, 1988
- Criteria for the Prenatal Diagnosis of HoloprosencephalyAmerican Journal of Perinatology, 1987
- A case of suspected teratogenic holoprosencephaly.Journal of Medical Genetics, 1985
- Single central incisor in familial holoprosencephalyThe Journal of Pediatrics, 1984
- What is the incidence of holoprosencephaly?Journal of Medical Genetics, 1984
- Holoprosencephaly in infants of diabetic mothersThe Journal of Pediatrics, 1983
- The developmental field concept in clinical geneticsThe Journal of Pediatrics, 1982
- Cyclopia and other anomalies following maternal ingestion of salicylatesThe Journal of Pediatrics, 1980
- Hypothalamic-pituitary dysfunction in siblings of patients with holoprosencephalyThe Journal of Pediatrics, 1973
- Familial holoprosencephaly with endocrine dysgenesisThe Journal of Pediatrics, 1968