Literature DB >> 18049080

Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorder.

Maria Leine Guion-Almeida1, Antonio Richieri-Costa, Roseli Maria Zechi-Ceide.   

Abstract

We report on three unrelated Brazilian patients with a holoprosencephaly phenotype, with variable central nervous system involvement, ano/microphthalmia, and first branchial arch anomalies. The features of these patients show a striking similarity to those of the patients reported by Guion-Almeida et al. (1999) and Ribeiro et al. (2005), thus confirming the existence of this rare condition. All cases are isolated and the etiology remains unknown.

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Year:  2008        PMID: 18049080     DOI: 10.1097/MCD.0b013e328274244f

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  2 in total

1.  Goldenhar syndrome in an infant of diabetic mother.

Authors:  Manizheh Mostafa Gharehbaghi; Mir-Reza Ghaemi
Journal:  Iran J Pediatr       Date:  2010-03       Impact factor: 0.364

Review 2.  The Molecular Basis of Human Anophthalmia and Microphthalmia.

Authors:  Philippa Harding; Mariya Moosajee
Journal:  J Dev Biol       Date:  2019-08-14
  2 in total

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