Literature DB >> 1789286

Prenatal ascertainment of an inherited dup(18p) associated with an apparently normal phenotype.

D J Wolff1, L J Raffel, M M Ferré, S Schwartz.   

Abstract

Direct two-generation transmission of an unbalanced 18p+ chromosome was discovered after amniocentesis. Neither the mother nor the child exhibited apparent physical malformations or mental impairment. Banding analysis suggested a complete 18p duplication. Molecular studies verified the 18p origin of the duplicated material. Only 14 previous cases of duplication 18p have been reported and these exhibited either a normal phenotype or mild and inconsistent abnormalities. The present cases, as well as the review of literature, indicate that duplication 18p is associated with few or inapparent phenotypic abnormalities.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1789286     DOI: 10.1002/ajmg.1320410311

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


  7 in total

1.  Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

Authors:  J C Barber; C A Joyce; M N Collinson; J C Nicholson; L R Willatt; H M Dyson; M S Bateman; A J Green; J R Yates; N R Dennis
Journal:  J Med Genet       Date:  1998-06       Impact factor: 6.318

2.  Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations.

Authors:  I A Glass; P Stormer; P T Oei; E Hacking; P D Cotter
Journal:  J Med Genet       Date:  1998-04       Impact factor: 6.318

3.  Clinical outcomes of adjacent 1 segregation in a familial translocation t(8;18)(p21.3;p11.23).

Authors:  A E Cockwell; R S James; I E Moore; E Hatchwell; J A Crolla
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

4.  Genetic determinants of autism in individuals with deletions of 18q.

Authors:  Louise O'Donnell; Bridgette Soileau; Patricia Heard; Erika Carter; Courtney Sebold; Jon Gelfond; Daniel E Hale; Jannine D Cody
Journal:  Hum Genet       Date:  2010-05-25       Impact factor: 4.132

Review 5.  Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.

Authors:  J C K Barber
Journal:  J Med Genet       Date:  2005-08       Impact factor: 6.318

Review 6.  Chromosome abnormalities without phenotypic consequences.

Authors:  Małgorzata Kowalczyk; Małgorzata Srebniak; Agnieszka Tomaszewska
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

7.  Azoospermia and trisomy 18p syndrome: a fortuitous association? A patient report and a review of the literature.

Authors:  Guillaume Jedraszak; Henri Copin; Manuel Demailly; Catherine Quibel; Thierry Leclerc; Marlène Gallet; Moncef Benkhalifa; Aline Receveur
Journal:  Mol Cytogenet       Date:  2015-06-04       Impact factor: 2.009

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.