Holoprosencephaly survival and performance

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 89, Issue 2, 1999, Pages 116-120

  Barr Jr , Mason ^a   Cohen Jr , M Michael ^b  

^a UNIVERSITY OF MICHIGAN HOSPITALS   (United States)

^b NONE

Author keywords

Cyclopia; Holoprosencephaly; Premaxillary agenesis; Survival study

Indexed keywords

ANOSMIA; ARTICLE; BRAIN STEM INJURY; CHILD; CYCLOPIA; DEVELOPMENTAL DISORDER; FAMILY COUNSELING; HOLOPROSENCEPHALY; HUMAN; INFANT; MUSCLE TONE; PRIORITY JOURNAL; SEIZURE; SURVIVAL;

BRAIN; BRAIN STEM; DEVELOPMENTAL DISABILITIES; HOLOPROSENCEPHALY; HUMANS; INFANT; INFANT, NEWBORN; INFECTION; OLFACTION DISORDERS; SURVIVAL RATE;

EID: 0342827846     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990625)89:2<116::AID-AJMG10>3.0.CO;2-4     Document Type: Article

References (4)

1. Barkovich AJ, Quint DJ. 1993. Middle interhemispheric fusion: an unusual variant of holoprosencephaly. Am J Neuroradiol 14: 31-440.
2. Cohen MM, Fraser FC, Gorlin RJ. 1990. Craniofacial disorders. In: Emery AEH, Rimoin DL, editors. Principles and practice of medical genetics, vol. 1. Edinburgh: Churchill Livingstone. p 749-796.
3. Croen LA, Shaw GM, Lammer EJ. 1996. Holoprosencephaly epidemiologic and clinical characteristics of a California population. Am J Med Genet 64:465-472.
4. Roach E, DeMyer W, Conneally PM, Palmer C, Meritt AD. 1975. Holoprosencephaly: birth data, genetic and demographic analyses of 30 families. BD:OAS 11(2):294-313.