A Case Report of Dyschromatosis Symmetrica Hereditaria with Glucose-6-Phosphate Dehydrogenase Deficiency

被引：0
|
作者：
Wang, Panpan [1 ]
Tang, Chenyu [1 ]
Zhao, Yige [1 ]
Wang, Ping [2 ]
机构：
[1] Zhejiang Chinese Med Univ, Hangzhou Peoples Hosp 3, Dept Dermatol, Hangzhou, Peoples R China
[2] Zhejiang Univ, Hangzhou Peoples Hosp 3, Dept Dermatol, Hangzhou Dermatol Hosp,Sch Med, Westlake Ave 38, Hangzhou, Peoples R China
来源：
CLINICAL COSMETIC AND INVESTIGATIONAL DERMATOLOGY | 2023年 / 16卷
关键词：
dyschromatosis symmetrica hereditaria; glucose-6-phosphate dehydrogenase deficiency; psychosis; ADAR1; MUTATIONS; GENE;
D O I：
10.2147/CCID.S407052
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
Dyschromatosis symmetrica hereditaria (DSH) is a pigmented genetic skin disorder with an incompletely understood pathogenesis characterized by reticular hyper-and hypopigmented skin patches on the dorsal aspect of the extremities, freckle-like patches on the face, and unaffected palms and feet. There is no effective treatment available. Glucose-6-phosphate dehydrogenase (G6PD) deficiency has not been reported in the literature of DSH. We describe for the first time a case of DSH with G6PD deficiency and a family history of psychosis.
引用
收藏
页码：1047 / 1050
页数：4
相关论文
共 50 条
  • [1] Dyschromatosis symmetrica hereditaria: report of a sporadic case
    Consigli, Javier
    Gomez Zanni, Maria S.
    Ragazzini, Luciana
    Danielo, Cristian
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2010, 49 (08) : 918 - 920
  • [2] Dermoscopic features in a case of dyschromatosis symmetrica hereditaria
    Oiso, Naoki
    Murata, Ichidai
    Hayashi, Masahiro
    Amatsu, Akinori
    Yoshida, Masuki
    Suzuki, Tamio
    Kawada, Akira
    JOURNAL OF DERMATOLOGY, 2011, 38 (01) : 91 - 93
  • [3] Glucose-6-phosphate dehydrogenase deficiency
    Sasmaz, Ilgen
    TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 2009, 44 : 35 - 38
  • [4] Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review
    Peng, Amy Chia-Ying
    Chen, Yi-An
    Chao, Sheau-Chiou
    DERMATOLOGICA SINICA, 2013, 31 (01) : 19 - 24
  • [5] Glucose-6-phosphate dehydrogenase deficiency in newborns in Argentina
    Federico Suldrup, Niels Alejandro
    Cesari, Natalia
    Raul Streitenberger, Edgardo
    Naretto, Antonela
    ACTA BIOQUIMICA CLINICA LATINOAMERICANA, 2014, 48 (02): : 169 - 182
  • [6] Glucose-6-phosphate dehydrogenase deficiency and stroke outcomes
    Ou, Zilin
    Chen, Yicong
    Li, Jianle
    Ouyang, Fubing
    Liu, Gang
    Tan, Shuangquan
    Huang, Weixian
    Gong, Xiao
    Zhang, Yusheng
    Liang, Zhijian
    Deng, Weisheng
    Xing, Shihui
    Zeng, Jinsheng
    NEUROLOGY, 2020, 95 (11) : E1471 - E1478
  • [7] Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Pakistani population
    Moiz, B.
    Nasir, A.
    Moatter, T.
    Naqvi, Z. A.
    Khurshid, M.
    INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, 2011, 33 (06) : 570 - 578
  • [8] Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency among Jordanians
    Al-Sweedan, Suleimman A.
    Awwad, Nor
    ACTA HAEMATOLOGICA, 2012, 128 (04) : 195 - 202
  • [9] Glucose-6-phosphate dehydrogenase deficiency in Tunisian jaundiced neonates
    Dabboubi, Rym
    Amri, Yessine
    Hamdi, Soumaya
    Jouini, Hamida
    Sahli, Chaima
    Fredj, Sondess Hadj
    Ben Salem, Kamel
    ElhoudaToumi, Nour
    Messaoud, Taieb
    ANNALES DE BIOLOGIE CLINIQUE, 2020, 78 (04) : 411 - 416
  • [10] Glucose-6-phosphate dehydrogenase deficiency: the added value of cytology
    Roelens, Marie
    Dossier, Claire
    Fenneteau, Odile
    Couque, Nathalie
    Da Costa, Lydie
    ANNALES DE BIOLOGIE CLINIQUE, 2016, 74 (03) : 299 - 305
12345