Literature DB >> 17985375

Cerebro-oculo-nasal syndrome: 13 new Brazilian cases.

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

Abstract

Cerebro-oculo-nasal syndrome (CONS) is characterized by structural anomalies of the central nervous system (encephalocele, ventricular dilatation, defects of corpus callosum, and even holoprosencephaly in one instance), by ocular alterations ranging from anophthalmia/microphthalmia to normal eyes, and by proboscis-like nares. Here, we report on 13 new cases with CONS, review 7 previously published cases, and evaluate the findings in all 20 patients. Despite marked variability among cases, the nasal configuration appears to be unique and diagnostic. Although one patient had a mutation in the PTCH gene, the cause of all other cases remains unknown to date. (c) 2007 Wiley-Liss, Inc.

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Year:  2007        PMID: 17985375     DOI: 10.1002/ajmg.a.32090

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  1 in total

1.  Correction of Unilateral Nostril Hypoplasia with Z-Plasty in a Child.

Authors:  Dong-Han Lee; Kap Sung Oh
Journal:  Arch Craniofac Surg       Date:  2014-08-14
  1 in total

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