Literature DB >> 7102721

Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).

R Voss, I Lerer, G Maftzir, M Sheinis, M M Cohen.   

Abstract

An abnormal karyotype consisting of 48 chromosomes has been found in a 16-year-old boy with severe psychomotor retardation and congenital anomalies. The two extra chromosomes: a 15q - and a small metacentric marker appear as derivatives of chromosome 15(48, XY, + 15q -, + mar(15). The healthy father has a mosaic chromosome constitution 46, XY/47, XY, + mar(15) and this additional chromosome is also present in the propositus. It is suggested that the presence of the extra chromosome in the father's germ cells may play a role in the production of the additional 15q - chromosome responsible for the clinical syndrome of the propositus.

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Year:  1982        PMID: 7102721     DOI: 10.1002/ajmg.1320120203

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


  3 in total

Review 1.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

2.  Supernumerary microchromosomes identified as inverted duplications of chromosome 15: a report of three cases.

Authors:  L P Wisniewski; R A Doherty
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Partial trisomy of chromosome 15q and partial monopsony of 6q due to maternal balanced translocation.

Authors:  Shilpy Singla; Kausik Mandal; Suvasini Sharma; Viswas Chhapola
Journal:  J Pediatr Neurosci       Date:  2014-05
  3 in total

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