Literature DB >> 7762587

Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.

P G Wheeler1, D D Weaver, C G Palmer.   

Abstract

A chromosomal translocation between chromosomes 4 and 8 resulting in Wolf-Hirschhorn syndrome in 2 individuals has been traced through 4 generations of a family. Ascertainment of the family was through a newborn infant with evident Wolf-Hirschhorn syndrome who had an unbalanced chromosomal translocation [46,XY,-4,+der(4),t(4;8) (p15.32;p22)]. Discussion with the family documented a paternal great-uncle who also had a similar phenotype and profound mental retardation. Subsequently this individual was found to have the same unbalanced chromosome constitution as the propositus. The 39-year-old great-uncle is the oldest reported individual with the Wolf-Hirschhorn syndrome. The importance of chromosome evaluation of older individuals with mental retardation syndromes is emphasized.

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Year:  1995        PMID: 7762587     DOI: 10.1002/ajmg.1320550414

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


  2 in total

1.  Translocations involving 4p16.3 in three families: deletion causing the Pitt-Rogers-Danks syndrome and duplication resulting in a new overgrowth syndrome.

Authors:  M W Partington; K Fagan; V Soubjaki; G Turner
Journal:  J Med Genet       Date:  1997-09       Impact factor: 6.318

2.  Mouse model implicates GNB3 duplication in a childhood obesity syndrome.

Authors:  Ian S Goldlust; Karen E Hermetz; Lisa M Catalano; Richard T Barfield; Rebecca Cozad; Grace Wynn; Alev Cagla Ozdemir; Karen N Conneely; Jennifer G Mulle; Shikha Dharamrup; Madhuri R Hegde; Katherine H Kim; Brad Angle; Alison Colley; Amy E Webb; Erik C Thorland; Jay W Ellison; Jill A Rosenfeld; Blake C Ballif; Lisa G Shaffer; Laurie A Demmer; M Katharine Rudd
Journal:  Proc Natl Acad Sci U S A       Date:  2013-08-26       Impact factor: 11.205

  2 in total

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