Dyschromatosis Universalis Hereditaria: A Unique Disorder-Reference-Cited by-同舟云学术

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Dyschromatosis Universalis Hereditaria: A Unique Disorder

Published:2000-01 Issue:1 Volume:17 Page:70-72
ISSN:0736-8046
Container-title:Pediatric Dermatology
language:en
Short-container-title:Pediatric Dermatology

Author:

Sethuraman Gomathy¹,Thappa Devinder M.¹,Vijaikumar ¹,Kumar Jeevan¹,Srinivasan Sadagopan¹

Affiliation:

1. Pondicherry, India

Publisher

Wiley

Subject

Dermatology,Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Dyschromatosis: Its Occurrence in Two Indian Families with Unusual Features

2. Dsychromatosis Symmetrica Hereditaria in an Indian Family

3. Universal dyschromatosis, small stature and high-tone deafness

4. Dyschromatosis universalis hereditaria.;Sait MA;Indian J Dermatol Venereol Leprol,1985

5. Dyschromatosis universalis hereditaria with epilepsy.;Pavithran K;Indian J Dermatol Venereol Leprol,1991

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing;Chinese Medical Journal;2016-01-05

2. Dyschromatosis universalis hereditaria: a case report;International Journal of Dermatology;2013-12-10

3. Amyloidosis cutis dyschromica;Orphanet Journal of Rare Diseases;2012-12

4. Amyloidosis cutis dyschromica: four cases from two families;International Journal of Dermatology;2009-05

5. Dyschromatosis universalis hereditaria: two cases in a Chinese family;Clinical and Experimental Dermatology;2005-09

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