Literature DB >> 10564882

Two sisters with Toriello-Carey syndrome.

Y Chinen1, T Tohma, Y Izumikawa, H Taketomi, T Iha, T Ohta, K Naritomi.   

Abstract

Toriello-Carey syndrome comprises agenesis of the corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, Robin sequence, abnormally shaped ears, cardiac defect, and hypotonia. We describe two Japanese sisters with a Toriello-Carey syndrome whose phenotypes were as severe as reported male cases. The younger sister died suddenly at age 4 months. Our patients with a severe phenotype and possible parental consanguinity suggest autosomal recessive inheritance of Toriello-Carey syndrome. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10564882     DOI: 10.1002/(sici)1096-8628(19991126)87:3<262::aid-ajmg13>3.0.co;2-3

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


  1 in total

1.  A novel multiple congenital anomaly-mental retardation syndrome with Pierre Robin sequence and cerebellar hypoplasia in two sisters.

Authors:  David A Stevenson; John C Carey
Journal:  Am J Med Genet A       Date:  2007-10-01       Impact factor: 2.802

  1 in total

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