A case of familial incontinentia pigmenti in infancy without hyperpigmented stage

作     者：Yumeng Wang Xinyi Wang Ting Chen Chaolan Pan Ming Li 

作者机构：Dermatology CenterXinhua HospitalShanghai Jiao Tong University School of MedicineShanghaiChina Department of DermatologyXinhua HospitalSchool of MedicineShanghai Jiao Tong UniversityShanghaiChina Institute of DermatologySchool of MedicineShanghai Jiao Tong UniversityShanghaiChina Department of DermatologyMinhang HospitalFudan UniversityShanghaiChina Department of DermatologyAffiliated Shenzhen Maternity&Child Healthcare HospitalSouthern Medical UniversityGuandongChina Department of DermatologyChildren’s Hospital of Fudan UniversityShanghaiChina 

出 版 物：《Pediatric Investigation》 (儿科学研究（英文）)

年 卷 期：2023年第7卷第3期

页      面：220-221页

核心收录：

学科分类：1003[医学-口腔医学] 1002[医学-临床医学] 100302[医学-口腔临床医学] 10[医学] 

基　　金：supported by the National Nature Science Foundation(82073422 and 82273504) the Shanghai Municipal Natural Science Foundation(22ZR1440800) 

主　　题：continent familial editor 

摘      要：To the editor:Incontinentia pigmenti(IP)is a rare X-linked dominant neuroectodermal disorder primarily caused by mutations in the IKBKG(NEMO)*** manifestations of IP typically progress through four stages:inflammatory(or vesicular)stage,verrucous stage,hyperpigmented stage,and hypopigmented(or atropic)stage.^(1)Throughout the disease course,most cases develop linear or whorled brownish reticular pigmentation following the lines of ***,some patients experience linear hypopigmentation and absence of hair,usually during ***,we report a rare manifestation of this disease.