Literature DB >> 7426420

Familial acrogeria (Gottron).

W P de Groot, J Tafelkruyer, M J Woerdeman.   

Abstract

A mother and her oldest son suffering from acrogeria are described; in the mother the disease was complicated by elastosis perforans serpiginosa. Microscopic and ultramicroscopic details are given.

Entities:  

Mesh：

Year:  1980        PMID： 7426420     DOI： 10.1111/j.1365-2133.1980.tb06595.x

Source DB:  PubMed          Journal:  Br J Dermatol        ISSN： 0007-0963            Impact factor:   9.302


  4 in total

1.  A rare case of acrogeria.

Authors:  Sunil Sanghi; R S Grewal; Biju Vasudevan; A Nagure
Journal:  Med J Armed Forces India       Date:  2013-04-08

2.  Skeletal abnormalities of acrogeria, a progeroid syndrome.

Authors:  A Ho; S J White; J E Rasmussen
Journal:  Skeletal Radiol       Date:  1987       Impact factor: 2.199

3.  Lymphocyte proliferation and nucleoid sedimentation in a case of premature aging distinct from Werner's syndrome.

Authors:  M A Kim; R Happle; H Traupe
Journal:  Arch Dermatol Res       Date:  1986       Impact factor: 3.017

Review 4.  Gottron's acrogeria and sarcoidosis.

Authors:  A Meurer; G Lohmöller; C Keller
Journal:  Clin Investig       Date:  1993-05
  4 in total

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