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Familial progressive hypo- and hyperpigmentation: a variant case.
Indian J Dermatol Venereol Leprol. 2012 May-Jun; 78(3):350-3.IJ

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.

Authors+Show Affiliations

The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.No affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

22565436

Citation

Zhang, Ru-zhi, and Wen-yuan Zhu. "Familial Progressive Hypo- and Hyperpigmentation: a Variant Case." Indian Journal of Dermatology, Venereology and Leprology, vol. 78, no. 3, 2012, pp. 350-3.
Zhang RZ, Zhu WY. Familial progressive hypo- and hyperpigmentation: a variant case. Indian J Dermatol Venereol Leprol. 2012;78(3):350-3.
Zhang, R. Z., & Zhu, W. Y. (2012). Familial progressive hypo- and hyperpigmentation: a variant case. Indian Journal of Dermatology, Venereology and Leprology, 78(3), 350-3. https://doi.org/10.4103/0378-6323.95453
Zhang RZ, Zhu WY. Familial Progressive Hypo- and Hyperpigmentation: a Variant Case. Indian J Dermatol Venereol Leprol. 2012 May-Jun;78(3):350-3. PubMed PMID: 22565436.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Familial progressive hypo- and hyperpigmentation: a variant case. AU - Zhang,Ru-zhi, AU - Zhu,Wen-yuan, PY - 2012/5/9/entrez PY - 2012/5/9/pubmed PY - 2012/9/5/medline SP - 350 EP - 3 JF - Indian journal of dermatology, venereology and leprology JO - Indian J Dermatol Venereol Leprol VL - 78 IS - 3 N2 - 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. SN - 0973-3922 UR - https://wwww.unboundmedicine.com/medline/citation/22565436/Familial_progressive_hypo__and_hyperpigmentation:_a_variant_case_ L2 - http://www.ijdvl.com/article.asp?issn=0378-6323;year=2012;volume=78;issue=3;spage=350;epage=353;aulast=Zhang DB - PRIME DP - Unbound Medicine ER -