Literature DB >> 12239716

Autosomal recessive alobar holoprosencephaly with essentially normal faces.

Mason Barr1, M Michael Cohen.   

Abstract

Holoprosencephaly is associated with a diagnostic face approximately 80% of the time. We report three siblings with alobar holoprosencephaly and essentially normal faces. A similar family was reported by Khan et al. [1970: Dev Med Child Neurol 12:71-76]. Alobar holoprosencephaly with essentially normal faces has also been observed in infants of diabetic mothers [Barr et al., 1983: J Pediatr 102:565-568]. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12239716     DOI: 10.1002/ajmg.10587

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  3 in total

1.  Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE.

Authors:  Jill A Rosenfeld; Blake C Ballif; Donna M Martin; Arthur S Aylsworth; Bassem A Bejjani; Beth S Torchia; Lisa G Shaffer
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

2.  Holoprosencephaly with multiple anomalies of the craniofacial bones-an autopsy report.

Authors:  E Aruna; V Kalyan Chakravarthy; D Naveen Chandar Rao; D Ranga Rao
Journal:  J Clin Diagn Res       Date:  2013-08-01

3.  Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report.

Authors:  Mosiany L Kisipan; Samuel N Nyaga; Jesse N Thuo; Phillip O Nyakego; Caleb O Orenge; Rodi O Ojoo
Journal:  Vet Med Sci       Date:  2020-01-23
  3 in total

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