Literature DB >> 823955

Reticulate acropigmentation of Kitamura.

W A Griffiths.   

Abstract

Seven cases of reticulate acropigmentation of Kitamura (RAPK) are described. All the patients were female and the pattern of inheritance suggested an autosomal dominant mode. Histologically, RAPK is characterized by epidermal atrophy, an increased number of basal melanocytes and the absence of pigmentary incontinence in the upper dermis. The present cases, from Asia, Africa and Europe, are the first to be described outside Japan.

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Year:  1976        PMID: 823955     DOI: 10.1111/j.1365-2133.1976.tb00848.x

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


  4 in total

1.  Reticulate acropigmentation of Kitamura: A familial case with eyelid involvement.

Authors:  Preema Sinha; Anamika Sinha; Sukriti Baveja; Manas Chatterjee
Journal:  Med J Armed Forces India       Date:  2014-08-14

2.  A Case of Reticulate Acropigmentation of Kitamura Treated with 532-nm Q-Switched Nd:YAG Laser: 10 Years of Follow-Up Observation.

Authors:  Jae Hyung Lee; Jong Hee Lee; Joo Heung Lee
Journal:  Ann Dermatol       Date:  2014-11-26       Impact factor: 1.444

3.  Pathogenicity of POFUT1 in Dowling-Degos disease: additional mutations and clinical overlap with reticulate acropigmentation of kitamura.

Authors:  F Buket Basmanav; Günter Fritz; Gilles G Lestringant; Divya Pachat; Sabine Hoffjan; Johannes Fischer; Maria Wehner; Sabrina Wolf; Holger Thiele; Janine Altmüller; Susanne A Pulimood; Arno Rütten; Roland Kruse; Sandra Hanneken; Jorge Frank; Sumita Danda; Anette Bygum; Regina C Betz
Journal:  J Invest Dermatol       Date:  2014-09-17       Impact factor: 8.551

Review 4.  Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders.

Authors:  H Alshaikh; F Alsaif; S Aldukhi
Journal:  Dermatol Res Pract       Date:  2017-10-23
  4 in total

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