Literature DB >> 8387739

Familial multiple glomangiomas.

R Rudolph1.   

Abstract

A 17-year-old patient had painful multiple glomangiomas, with an exceptionally strong family history extending back five generations. The mode of genetic transmission appeared to be autosomal dominant with complete gene penetrance. Simple excision provided symptom relief.

Entities:  

Mesh：

Year:  1993        PMID： 8387739     DOI： 10.1097/00000637-199302000-00017

Source DB:  PubMed          Journal:  Ann Plast Surg        ISSN： 0148-7043            Impact factor:   1.539


  4 in total

1.  Glomuvenous Malformation of the Neck.

Authors:  Muhammad Salman Khan; Amir Humza Sohail; Kiran Hilal; Muhammad Hassaan Arif Maan
Journal:  Int J Angiol       Date:  2019-08-06

2.  Mutations in a novel factor, glomulin, are responsible for glomuvenous malformations ("glomangiomas").

Authors:  Pascal Brouillard; Laurence M Boon; John B Mulliken; Odile Enjolras; Michella Ghassibé; Matthew L Warman; O T Tan; Bjorn R Olsen; Miikka Vikkula
Journal:  Am J Hum Genet       Date:  2002-02-13       Impact factor: 11.025

3.  A gene for inherited cutaneous venous anomalies ("glomangiomas") localizes to chromosome 1p21-22.

Authors:  L M Boon; P Brouillard; A Irrthum; L Karttunen; M L Warman; R Rudolph; J B Mulliken; B R Olsen; M Vikkula
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

4.  Genetic syndromes with vascular malformations - update on molecular background and diagnostics.

Authors:  Adam Ustaszewski; Joanna Janowska-Głowacka; Katarzyna Wołyńska; Anna Pietrzak; Magdalena Badura-Stronka
Journal:  Arch Med Sci       Date:  2020-02-25       Impact factor: 3.318
  4 in total

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