Literature DB >> 7471508

Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter).

J Stamberg, J Shapiro, D Valle, F P Kuhajda, G Thomas, L Wissow.   

Abstract

We report a stillborn infant with partial trisomy 6q who had several major congenital malformations not previously associated with the chromosomal aberration. These included occipital encephalocele, ambiguous genitalia with imperforate anus, omphalocele and unilateral hydronephrosis. The infant's karyotype was 46,XY,-22,der(22),t(6;22)(q21; p13) or (q21;pter)mat. The mother and maternal grandmother are balanced translocation carriers.

Entities:  

Mesh:

Year:  1981        PMID: 7471508     DOI: 10.1111/j.1399-0004.1981.tb00681.x

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


  2 in total

Review 1.  Partial duplication of the long arm of chromosome 6: a clinically recognisable syndrome.

Authors:  E K Pivnick; M B Qumsiyeh; A T Tharapel; J B Summitt; R S Wilroy
Journal:  J Med Genet       Date:  1990-08       Impact factor: 6.318

2.  A paternal t(6;22)(q25.3;p12) leading to a deleted and satellited der(6) in a short-lived infant.

Authors:  María Guadalupe Domínguez; Horacio Rivera; Rosa María Dávalos-Pulido; Ingrid Patricia Dávalos-Rodríguez
Journal:  J Clin Lab Anal       Date:  2020-05-12       Impact factor: 2.352

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.