Literature DB >> 7625434

Family with partial monosomy 10p and trisomy 10p.

E Hon1, C Chapman, T R Gunn.   

Abstract

We report on a family with an abnormality of 10p. The propositus has monosomy for the distal region of 10p and severe psychomotor delay, growth failure, congenital heart defect, multicystic kidney, grade V vesicoureteric reflux, and neurosensory hearing loss. The mother and the elder brother of the propositus carry a balanced reciprocal translocation (5q;10p)(q35.3;p12.3). A retarded and epileptic maternal aunt was found to have dup(10p). Study of the family history led to the successful obstetric management of a subsequent twin pregnancy in which an affected fetus with dup(10p) was identified and selectively terminated, while the other normal twin was delivered at term without problems.

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Year:  1995        PMID: 7625434     DOI: 10.1002/ajmg.1320560204

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


  3 in total

Review 1.  An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14.

Authors:  P Lichtner; R König; T Hasegawa; H Van Esch; T Meitinger; S Schuffenhauer
Journal:  J Med Genet       Date:  2000-01       Impact factor: 6.318

2.  MRI findings in a patient with partial monosomy 10p.

Authors:  F Sunada; F C Rash; D A Tam
Journal:  J Med Genet       Date:  1998-02       Impact factor: 6.318

3.  De novo Xp terminal deletion in a triple X female with recurrent spontaneous abortions: a case report.

Authors:  Tahir M Malla; Arshad A Pandith; Fayaz A Dar; Mahrukh H Zargar; Zafar A Shah
Journal:  J Genet       Date:  2014-12       Impact factor: 1.166

  3 in total

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