An unusual Case of Segmental Hailey-Hailey Disease Developing in a 1.5-Year-Old Child: A Proposed Diagnosis.
作者信息
Happle Rudolf
机构信息
Department of Dermatology, Medical Center-University of Freiburg, Freiburg, Germany E-mail:
出版信息
Indian J Dermatol. 2022 Jan-Feb;67(1):70-71. doi: 10.4103/ijd.ijd_152_21.
Abstract
摘要
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本文引用的文献
1
A Rare Case of Childhood-Onset Hailey-Hailey Disease at an Unusual Site.一例罕见的儿童期发病、部位特殊的黑棘皮病。 （注：你提供的原文病症名有误，正确病症名应该是“Hailey-Hailey disease”即“遗传性良性天疱疮”，按照正确病症名翻译为：一例罕见的儿童期发病、部位特殊的遗传性良性天疱疮。 ）
Indian J Dermatol. 2021 Jan-Feb;66(1):92-93. doi: 10.4103/ijd.IJD_626_19.
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Superimposed mosaicism in tuberous sclerosis complex: a key to understanding all of the manifold manifestations?结节性硬化症中的叠加镶嵌现象：理解所有多样临床表现的关键？
J Eur Acad Dermatol Venereol. 2020 Nov;34(11):2511-2517. doi: 10.1111/jdv.16603. Epub 2020 Jul 21.
3
Relapsing linear acantholytic dermatosis in a four-year-old boy.一名四岁男孩的复发性线状棘层松解性皮肤病。
Indian J Dermatol Venereol Leprol. 2005 Sep-Oct;71(5):351-3. doi: 10.4103/0378-6323.16789.
4
Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept.等位基因缺失是2型节段性黑棘皮病的基础，为一种新的遗传学概念提供了分子学证据。
J Clin Invest. 2004 Nov;114(10):1467-74. doi: 10.1172/JCI21791.
5
Relapsing linear acantholytic dermatosis.
Br J Dermatol. 1985 Mar;112(3):349-55. doi: 10.1111/j.1365-2133.1985.tb04864.x.
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