Successful treatment of early-onset hidradenitis suppurativa with acitretin in an infant with a novel mutation in PSENEN gene

被引：6
|
作者：
Chen, An-Wei [1 ]
Chen, Zhi [1 ]
Bai, Xiao-Ming [2 ]
Luo, Xiao-Yan [3 ]
Wang, Hua [4 ]
机构：
[1] Chongqing Med Univ, Chongqing Key Lab Child Infect & Immun, Chongqing, Peoples R China
[2] Chongqing Med Univ, Key Lab Child Dev & Disorders, Minist Educ, Chongqing, Peoples R China
[3] Chongqing Med Univ, China Int Sci & Technol Cooperat Base Child Dev, Chongqing, Peoples R China
[4] Chongqing Med Univ, Dept Dermatol, Childrens Hosp, 136,Zhongshan 2nd Rd, Chongqing 400014, Peoples R China
来源：
INDIAN JOURNAL OF DERMATOLOGY VENEREOLOGY & LEPROLOGY | 2022年 / 88卷 / 03期
关键词：
ACNE INVERSA;
D O I：
10.25259/IJDVL_471_19
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：445 / +
页数：3
相关论文
共 50 条
  • [21] Novel Therapy for the Treatment of Early-Onset Preeclampsia
    Ornaghi, Sara
    Paidas, Michael J.
    CLINICAL OBSTETRICS AND GYNECOLOGY, 2017, 60 (01): : 169 - 182
  • [22] Novel NFKB2 Mutation in Early-Onset CVID
    Yiwen Liu
    Steven Hanson
    Padmalal Gurugama
    Alison Jones
    Barnaby Clark
    Mohammad A A Ibrahim
    Journal of Clinical Immunology, 2014, 34 : 686 - 690
  • [23] Novel NFKB2 Mutation in Early-Onset CVID
    Liu, Yiwen
    Hanson, Steven
    Gurugama, Padmalal
    Jones, Alison
    Clark, Barnaby
    Ibrahim, Mohammad A. A.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (06) : 686 - 690
  • [24] Early-onset ataxia with oculomotor apraxia with a novel APTX mutation
    Ito, A
    Yamagata, T
    Mori, M
    Momoi, MY
    PEDIATRIC NEUROLOGY, 2005, 33 (01) : 53 - 56
  • [25] Novel NFKB2 Mutation in Early-Onset CVID
    Liu, Y.
    Hanson, S.
    Gurugama, P.
    Jones, A.
    Clark, B.
    Ibrahim, M.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 : S429 - S430
  • [26] A novel point mutation in parkin gene was identified in an early-onset case of Parkinson's disease
    Wang, Tao
    Liang, Zhi-hou
    Sun, Sheng-gang
    Cao, Xue-bing
    Peng, Hai
    Cao, Fei
    Liu, Hongjin
    Tong, E-tang
    Chinese Journal of Medical Genetics, 2003, 20 (02) : 111 - 113
  • [27] Identification of a novel mutation in APP gene in a Thai subject with early-onset Alzheimer's disease
    Vo Van Giau
    Senanarong, Vorapun
    Bagyinszky, Eva
    Limwongse, Chanin
    An, Seong Soo A.
    Kim, SangYun
    NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2018, 14 : 3015 - 3023
  • [28] Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation
    Qian, Yanyan
    Wu, Bingbing
    Lu, Yulan
    Dong, Xinran
    Qin, Qian
    Zhou, Wenhao
    Wang, Huijun
    COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2018, 4 (06):
  • [29] Early-onset obesity in the setting of a ULK4 gene mutation
    Greene, Elizabeth
    Page, Laura
    HORMONE RESEARCH IN PAEDIATRICS, 2022, 95 (SUPPL 1): : 123 - 124
  • [30] An updated mutation spectrum of the γ-secretase complex: Novel NCSTN gene mutation in an Indian family with hidradenitis suppurativa and acne conglobata
    Ratnamala, Uppala
    Jain, Nayan K.
    Jhala, Devendrasinh D.
    Prasad, Pullabatla V. S.
    Saiyed, Nazia
    Nair, Sreelatha
    Radhakrishna, Uppala
    INDIAN JOURNAL OF DERMATOLOGY, 2023, 68 (02) : 141 - 147
12345