Acral dyschromatosis with developmental regression and dystonia in a seven- year-old child: Dyschromatosis symmetrica hereditaria variant or a new syndrome

被引：8

作者：

Kaliyadan, Feroze ^{[1
]}

Vinayan, K. P. ^{[2
]}

Fernandes, Bindiya ^{[1
]}

Jayasree, M. G. ^{[3
]}

机构：

[1] Amrita Inst Med Sci, Dept Dermatol, Kochi 682028, Kerala, India

[2] Amrita Inst Med Sci, Dept Pediat Neurol, Kochi 682028, Kerala, India

[3] Amrita Inst Med Sci, Dept Pathol, Kochi 682028, Kerala, India

来源：

关键词：

MUTATIONS; FAMILY; GENE;

D O I：

10.4103/0378-6323.53154

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：412 / 414

页数：3

共 7 条

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[6] Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation
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[7] Dyschromatosis
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