Literature DB >> 4085142

Partial trisomy 6p and partial monosomy 9p from a de novo translocation 46,XY, -9, +DER(9)T(6:9)(p211:p24).

M S Eden, J W Thelin, K Michalski, J A Mitchell.   

Abstract

This report describes an adult male with a partial trisomy 6p(p211-pter) and a partial monosomy 9p(9p24-pter) resulting from a de novo unbalanced translocation. This patient does not show the classical featured of the 9p partial monosomy syndrome, thus disputing the claim of Hoo et al. (1982) that 9p24 is the critical segment for the monosomy syndrome. Partial trisomy for 6p has only been previously reported in children. In addition to the chromosomal anomalies, the patient has autosomal recessive spinal muscular atrophy with a different age of onset than two affected sibs. Finally, he shows unusual audiologic and ophthalmologic signs nor previously reported as part of the 9p monosomy or 6p trisomy syndromes.

Entities:  

Mesh:

Year:  1985        PMID: 4085142     DOI: 10.1111/j.1399-0004.1985.tb02210.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

Review 1.  Eleven new cases of del(9p) and features from 80 cases.

Authors:  J L Huret; C Leonard; B Forestier; M O Rethoré; J Lejeune
Journal:  J Med Genet       Date:  1988-11       Impact factor: 6.318

2.  A Case Report of 9p Deletion Syndrome Associated with Partial Trisomy of 1q42.

Authors:  Ali Vahabi; Filiz Hazan; Isa Abdi Rad
Journal:  Maedica (Bucur)       Date:  2017-01

3.  Diagnostic Approach to Microdeletion Syndromes Based on 22q11.2 Investigation: Challenges in Four Cases.

Authors:  Ilária C Sgardioli; Matheus de Mello Copelli; Fabíola P Monteiro; Ana P Dos Santos; Elaine Lustosa Mendes; Társis Paiva Vieira; Vera L Gil-da-Silva-Lopes
Journal:  Mol Syndromol       Date:  2017-06-24
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.