Literature DB >> 3970841

Familial primary cutaneous amyloidosis.

J A Newton, A Jagjivan, B Bhogal, P H McKee, D H McGibbon.   

Abstract

Primary cutaneous amyloidosis is uncommon in Europeans. A British family is described in which an extremely rare variant was inherited as an autosomal dominant. The subtlety of physical signs in this family contrasted with the severity of the associated pruritus. Transepidermal elimination of amyloid was a characteristic histological feature.

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Year:  1985        PMID： 3970841     DOI： 10.1111/j.1365-2133.1985.tb00084.x

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


  6 in total

Review 1.  [Hereditary and non-hereditary cutaneous amyloidoses].

Authors:  S Schreml; J Schroeder; F Eder; R M Szeimies; M Landthaler; P Babilas
Journal:  Pathologe       Date:  2009-05       Impact factor: 1.011

2.  Bullous variant of familial biphasic lichen amyloidosis: a unique combination of three rare presentations.

Authors:  Vijayalaxmi Veerabasappa Suranagi; Bs Siddramappa; Hema Basappa Bannur; Prakash V Patil; Reshma S Davangeri
Journal:  Indian J Dermatol       Date:  2015 Jan-Feb       Impact factor: 1.494

3.  Novel IL31RA gene mutation and ancestral OSMR mutant allele in familial primary cutaneous amyloidosis.

Authors:  Ming-Wei Lin; Ding-Dar Lee; Tze-Tze Liu; Yong-Feng Lin; Shang-Yi Chen; Chih-Cheng Huang; Hui-Ying Weng; Yu-Fen Liu; Akio Tanaka; Ken Arita; Joey Lai-Cheong; Francis Palisson; Yun-Ting Chang; Chu-Kwan Wong; Isao Matsuura; John A McGrath; Shih-Feng Tsai
Journal:  Eur J Hum Genet       Date:  2010-01       Impact factor: 4.246

4.  In vitro amyloidogenic peptides of galectin-7: possible mechanism of amyloidogenesis of primary localized cutaneous amyloidosis.

Authors:  Koji Ono; Eita Fujimoto; Norihiro Fujimoto; Minoru Akiyama; Takahiro Satoh; Hiroki Maeda; Noriko Fujii; Shingo Tajima
Journal:  J Biol Chem       Date:  2014-08-29       Impact factor: 5.157

5.  Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis.

Authors:  Ken Arita; Andrew P South; Günter Hans-Filho; Thais Harumi Sakuma; Joey Lai-Cheong; Suzanne Clements; Maçanori Odashiro; Danilo Nakao Odashiro; Günter Hans-Neto; Nelise Ritter Hans; Maxine V Holder; Balbir S Bhogal; Sian T Hartshorne; Masashi Akiyama; Hiroshi Shimizu; John A McGrath
Journal:  Am J Hum Genet       Date:  2008-01       Impact factor: 11.025

6.  Hereditary amyloid cardiomyopathy caused by a variant apolipoprotein A1.

Authors:  L Hamidi Asl; J J Liepnieks; K Hamidi Asl; T Uemichi; G Moulin; E Desjoyaux; R Loire; M Delpech; G Grateau; M D Benson
Journal:  Am J Pathol       Date:  1999-01       Impact factor: 4.307
  6 in total

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