Progress in the Diagnosis and Treatment and the Establishment of Care System for Rare Skin Diseases
LIU Xiaohan, JIN Hongzhong
2023, 2(2): 147-152. DOI: 10.12376/j.issn.2097-0501.2023.02.001
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Work Progress and Outlook of Rare Skin Diseases Team
WU Chao, JIN Hongzhong
2023, 2(2): 153-156. DOI: 10.12376/j.issn.2097-0501.2023.02.002
Abstract PDF
Artificial Intelligence Applications in Rare Skin Diseases
WANG Yukun, LIU Jie
2023, 2(2): 157-163. DOI: 10.12376/j.issn.2097-0501.2023.02.003
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Research Development in Patients with Olmsted Syndrome
WEI Haoran, TAO Juan
2023, 2(2): 164-169. DOI: 10.12376/j.issn.2097-0501.2023.02.004
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Analysis of 8 Cases of Blau Syndrome/Early-onset Sarcoidosis——Clinical Manifestations, Histopathology Features and Gene Mutation Diversity
ZHENG Yi, JIA Tao, YAN Cong, ZHANG Xinyue, DU Xueshan, ZHOU Tong, SONG Xiangjin, GENG Songmei
2023, 2(2): 170-177. DOI: 10.12376/j.issn.2097-0501.2023.02.005
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Clinical Features and Mutation Analysis of the SMARCAD1 Gene in a Family with Basan Syndrome and a Literature Review
LIU Zhouliang, YANG Chao, WANG Huijun, LIN Zhimiao
2023, 2(2): 178-185. DOI: 10.12376/j.issn.2097-0501.2023.02.006
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Neurofibromatosis Type 1 in a Child with Plexiform Neurofibroma Pressing the Urinary System
XU Jianing, GUO Yaxin, WANG Shanshan, YIN Lei, ZHU Jiaming, CHENG Wen, JIANG Hongkun, GAO Xinghua, XU Xuegang
2023, 2(2): 186-190. DOI: 10.12376/j.issn.2097-0501.2023.02.007
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Expert Guidelines for the Diagnosis, Treatment, and Management of Mycosis Fungoides in China
Rare Skin Disease Committee of China Alliance for Rare Diseases, National Clinical Research Center for Dermatologic and Immunologic Diseases, Dermatology Branch of China International Exchange and Promotion Association for Medical and Health Care
2023, 2(2): 191-209. DOI: 10.12376/j.issn.2097-0501.2023.02.008
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Guidelines for the Multidisciplinary Diagnosis and Treatment of Neurofibromatosis Type 1(2023 Version)
Multidisciplinary Diagnosis and Treatment Collaboration Group for Neurofibromatosis Type 1 of China Alliance for Rare Diseases
2023, 2(2): 210-230. DOI: 10.12376/j.issn.2097-0501.2023.02.009
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Clinical Practice Guideline for Adolescent & Adult Patients with Spinal Muscular Atrophy
Rare Disease Society of Chinese Research Hospital Association, China Alliance for Rare Diseases, Beijing Society of Rare Disease Clinical Care and Accessibility, China Expert Group for Clinical Practice Guideline for Adolescent & Adult Patients with Spinal Muscular Atrophy
2023, 2(2): 231-255. DOI: 10.12376/j.issn.2097-0501.2023.02.010
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A Case of Paraneoplastic Pemphigus with Malignant Thymoma and Obliterated Bronchiolitis
WANG Rui, WANG Mingyue
2023, 2(2): 256-260. DOI: 10.12376/j.issn.2097-0501.2023.02.011
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Current Status and Prospect of Orphan Drugs for Rare Skin Diseases in China
ZHANG Shan, WU Chao, LIU Zhaorui, GAO Yimeng, LIU Jie, JIN Hongzhong
2023, 2(2): 261-272. DOI: 10.12376/j.issn.2097-0501.2023.02.012
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Progress in the Treatment of Topical Rapamycin Preparations
WANG Senfen, LIU Yuanxiang, XU Zigang
2023, 2(2): 273-280. DOI: 10.12376/j.issn.2097-0501.2023.02.013
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A Case Report of Nevus Trichilemmocysticus
LIU Ling, WANG Lei, WANG Gang
2023, 2(2): 281-284. DOI: 10.12376/j.issn.2097-0501.2023.02.014
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A Case Report of Annular Elastolytic Giant Cell Granuloma
QIAO Zusha, JIN Hongzhong
2023, 2(2): 285-289. DOI: 10.12376/j.issn.2097-0501.2023.02.015
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Mutations in CERS3 Gene Underlies a Case of Autosomal Recessive Congenital Ichthyosis
LIU Juan, MO Ran, LIU Yihe, HUANG Xin, GAO Meng, YANG Yong, CHEN Zhiming
2023, 2(2): 290-293. DOI: 10.12376/j.issn.2097-0501.2023.02.016
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Advances of Dupilumab in Treating Rare Monogenic Inherited Skin Diseases
ZHANG Yuqiao, ZENG Yueping
2023, 2(2): 294-302. DOI: 10.12376/j.issn.2097-0501.2023.02.017
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Advances of Congenital Alopecia/Hypotrichosis in Genetics Research
CUI Can, CHEN Xi, WEI Aihua
2023, 2(2): 303-312. DOI: 10.12376/j.issn.2097-0501.2023.02.018
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Advances in Pseudoxanthoma Elasticum
WANG Huifen, ZHAI Zhifang
2023, 2(2): 313-318. DOI: 10.12376/j.issn.2097-0501.2023.02.019
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