Literature DB >> 22565436

Familial progressive hypo- and hyperpigmentation: a variant case.

Ru-zhi Zhang1, Wen-yuan Zhu.   

Abstract

Familial progressive hyper- and hypopigmentation (FPHH) is characterized by diffuse hyperpigmentation with variable intensity. Cafe'-au-lait macules and larger hypopigmented ash-leaf macules are also present. Herein, we reported a variant case of FPHH. The patient was a two-year-old Chinese girl showing diffuse hyper- and hypopigmented lesions, longitudinal melanonychia in both thumbs, and infantile seizures, without any lentigines.

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Year:  2012        PMID: 22565436     DOI: 10.4103/0378-6323.95453

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  2 in total

1.  Familial progressive hyper- and hypopigmentation: a report on a Chinese family and evidence for genetic heterogeneity.

Authors:  Fang Xiao-Kai; He Yue-Xi; Li Yan-Jia; Chen Li-Rong; Wang He-Peng; Sun Qing
Journal:  An Bras Dermatol       Date:  2017 May-Jun       Impact factor: 1.896

2.  Identification of a novel mutation in the KITLG gene in a Chinese family with familial progressive hyper- and hypopigmentation.

Authors:  Jianbo Wang; Weisheng Li; Naihui Zhou; Jingliu Liu; Shoumin Zhang; Xueli Li; Zhenlu Li; Ziliang Yang; Miao Sun; Min Li
Journal:  BMC Med Genomics       Date:  2021-01-06       Impact factor: 3.063

  2 in total

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