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作 者:郑铭 吕小岩[1,2] ZHENG Ming;LYU Xiaoyan(Department of Dermatology,West China Hospital,Sichuan University,Chengdu 610041,China;Laboratory of Dermatology,Clinical Institute of Inflammation and Immunology,Frontiers Science Center for Disease-related Molecular Network,West China Hospital,Sichuan University,Chengdu 610041,China)
机构地区:[1]四川大学华西医院皮肤科,成都610041 [2]四川大学华西医院疾病分子网络前沿科学中心免疫炎症研究院皮肤病学研究室,成都610041
出 处:《中国麻风皮肤病杂志》2022年第10期717-719,共3页China Journal of Leprosy and Skin Diseases
摘 要:患者,男,4岁。脱发、全身丘疹伴畏光4年。基因检测示患儿MBTPS2基因有1个半合子突变,即c.3G>C(p.M1I)。母亲该位点杂合变异,父亲该位点无变异,诊断为毛囊性鱼鳞病-脱发-畏光综合征。A 4-year-old male presented with atrichia,papules and photophobia for 4 years.Genetic test identified a hemizygotic mutation of c.3G>C(p.M1I).The heterozygous mutation was found in the patient s mother and there was no mutation was found in the father.The diagnosis of ichthyosis follicularis,atrichia and photophobia syndrome was made.
关 键 词:毛囊性鱼鳞病-脱发-畏光综合征 MBTPS2基因 X连锁隐性遗传
分 类 号:R758.71[医药卫生—皮肤病学与性病学]
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