Literature DB >> 23498567

Monozygotic twins with trisomy 21 and partial agenesis of the corpus callosum.

Francois D Jacob1, Lori J Dobson, Judy A Estroff, Omar S Khwaja.   

Abstract

Trisomy 21 is the most common viable trisomy. Although it is invariably associated with mild to severe developmental delay and intellectual disability, no gross central nervous system malformation has been consistently identified in individuals with trisomy 21. We present the case of a monozygotic twin pregnancy in which both fetuses were identified as having trisomy 21 and partial agenesis of the corpus callosum. We discuss this rare association in the context of an emerging understanding of the neurobiology of trisomy 21.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23498567     DOI: 10.1016/j.pediatrneurol.2012.12.014

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  3 in total

Review 1.  Rare case of monozygotic twins diagnosed with klinefelter syndrome during evaluation for infertility.

Authors:  Yagil Barazani; Edmund Sabanegh
Journal:  Rev Urol       Date:  2015

2.  [Pediatric neurofunctional intervention in agenesis of the corpus callosum: a case report].

Authors:  Sheila Cristina da Silva Pacheco; Ana Paula Adriano Queiroz; Nathália Tiepo Niza; Letícia Miranda Resende da Costa; Lilian Gerdi Kittel Ries
Journal:  Rev Paul Pediatr       Date:  2014-10-03

3.  Prenatal genetic testing in 19 fetuses with corpus callosum abnormality.

Authors:  Qin She; Erfang Tang; Cui Peng; Li Wang; Dandan Wang; Weihe Tan
Journal:  J Clin Lab Anal       Date:  2021-09-27       Impact factor: 2.352

  3 in total

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