Literature DB >> 11170075

Hydrops fetalis in an interstitial deletion of chromosome 10.

R Jain1, C Jones.   

Abstract

We report the case of a premature neonate with ascites and dysmorphic facial features at birth. The chromosomal analysis showed an interstitial deletion of chromosome 10, that is, 46, XX, del(10)(q22.3q24.1). This is the first known case of a patient with interstitial deletion of chromosome 10 with symptoms of ascites and hydrops. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11170075     DOI: 10.1002/1096-8628(20010201)98:4<320::aid-ajmg1099>3.0.co;2-u

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


  1 in total

1.  A case report of chromosome 17q22-qter trisomy with distinct clinical presentation and review of the literature.

Authors:  Jariya Upadia; Joseph B Philips; Nathaniel H Robin; Edward J Lose; Fady M Mikhail
Journal:  Clin Case Rep       Date:  2018-02-14
  1 in total

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