Literature DB >> 1481852

Possible relationship between ulnar-mammary syndrome and split hand with aplasia of the ulna syndrome.

P Franceschini1, M P Vardeu, L Dalforno, F Signorile, D Franceschini, R Lala, P Matarazzo.   

Abstract

We describe a 3-generation family in which mother, maternal grandfather, and 2 (male and female) children have variably manifestations of the ulnar-mammary syndrome, including ulnar ray defects, obesity, hypogenitalism, delayed puberty, hypoplasia of nipples and apocrine glands, and a previously undescribed ectopia of upper canines. The index patient also had split-hand appearance on the right due to complete absence of the 4th ray. To our knowledge this is the first documented example of split hand in the ulnar-mammary syndrome. The hand anomaly raises the question of a possible causal relationship between ulnar-mammary syndrome and the split hand with aplasia of the ulna syndrome, as already hypothesized by Lenz [1980].

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Year:  1992        PMID: 1481852     DOI: 10.1002/ajmg.1320440618

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


  3 in total

1.  The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.

Authors:  M Bamshad; T Le; W S Watkins; M E Dixon; B E Kramer; A D Roeder; J C Carey; S Root; A Schinzel; L Van Maldergem; R J Gardner; R C Lin; C E Seidman; J G Seidman; R Wallerstein; E Moran; R Sutphen; C E Campbell; L B Jorde
Journal:  Am J Hum Genet       Date:  1999-06       Impact factor: 11.025

2.  Syndromic ectrodactyly with severe limb, ectodermal, urogenital, and palatal defects maps to chromosome 19.

Authors:  J R O'Quinn; R C Hennekam; L B Jorde; M Bamshad
Journal:  Am J Hum Genet       Date:  1998-01       Impact factor: 11.025

3.  Dynamic expression of Tbx2 subfamily genes in development of the mouse reproductive system.

Authors:  Nataki C Douglas; Kathleen Heng; Mark V Sauer; Virginia E Papaioannou
Journal:  Dev Dyn       Date:  2011-12-16       Impact factor: 3.780

  3 in total

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