Literature DB >> 3953673

Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata.

W Wertelecki, W R Breg, J M Graham, K Iinuma, S M Puck, F R Sergovich.   

Abstract

Mosaic trisomy 22, ascertained in three unrelated patients, was found to be associated with body asymmetry and signs of the Ullrich-Turner syndrome including short stature, ptosis, webbed neck, nevi, cubitus valgus, dysplastic nails, malformed great vessels, and abnormal ovaries. These anomalies in trisomy 22 mosaicism have not been emphasized heretofore. In each of our patients, trisomy 22 mosaicism was found only in fibroblasts. In one patient, the trisomy resulted from a paternal first meiotic nondisjunction, and in the 46,XX cells, both chromosomes 22 were of paternal origin.

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Year:  1986        PMID: 3953673     DOI: 10.1002/ajmg.1320230302

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


  2 in total

Review 1.  Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.

Authors:  I T Thomas; J L Frias; E S Cantu; C Z Lafer; D B Flannery; J G Graham
Journal:  Am J Hum Genet       Date:  1989-08       Impact factor: 11.025

2.  Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty.

Authors:  Shweta U Dhar; Patricia Robbins-Furman; Moise L Levy; Ankita Patel; Fernando Scaglia
Journal:  Am J Med Genet A       Date:  2009-05       Impact factor: 2.802

  2 in total

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