Literature DB >> 22585428

Novel clinical findings in a case of postnatally diagnosed trisomy 12 mosaicism.

Walla Al-Hertani1, Jean McGowan-Jordan, Judith E Allanson.   

Abstract

We report on a girl with trisomy 12 mosaicism diagnosed postnatally. She has been followed from 4 months of age for developmental delay, unilateral sensorineural hearing loss, intestinal malrotation, hemi-hyperplasia, pigmentary dysplasia, retinopathy, and a vascular ring. To our knowledge, there have been no reports of complete trisomy 12 in the literature. However there have been a few reports describing the phenotype of individuals with trisomy 12 mosaicism. This case report is a description of the eighth liveborn individual diagnosed postnatally with this condition.
Copyright © 2012 Wiley Periodicals, Inc.

Entities:  

Mesh:

Year:  2012        PMID: 22585428     DOI: 10.1002/ajmg.a.35354

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  2 in total

1.  Small bowel malrotation in distal 15q duplication: evidence for a rare association.

Authors:  Brooke M McLaughlin; Robert B Hufnagel; Howard M Saal
Journal:  Clin Dysmorphol       Date:  2015-04       Impact factor: 0.816

Review 2.  Mosaic trisomy 12 diagnosed in a female patient: clinical features, genetic analysis, and review of the literature.

Authors:  Daniela Hainz; Marcus Krüger; Daniela Reber; Karl Mehnert; Theresa Brunet; Gabriele Lederer; Sabine Langer-Freitag; Julia Hoefele
Journal:  World J Pediatr       Date:  2021-07-14       Impact factor: 2.764

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.