Dermatopathia pigmentosa reticularis: A rare case report and review of literature

Autor:	Aswath Rajan, Vivekbhai Itaiya, Simanthini Sakhardande, Varadharaj Pai, Pankaj Shukla
Jazyk:	angličtina
Rok vydání:	2022
Předmět:	adermatoglyphia alopecia dermatopathia pigmentosa reticularis dermoscopy hypohydrosis reticulate pigmentation Dermatology RL1-803
Zdroj:	Clinical Dermatology Review, Vol 6, Iss 1, Pp 54-54 (2022)
Druh dokumentu:	article
ISSN:	2542-551X 2542-5528
DOI:	10.4103/cdr.cdr_119_20
Popis:	Dermatopathia pigmentosa reticularis is a rare autosomal dominant disorder. It is an ectodermal dysplasia, characterized by a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. The mode of inheritance is probably autosomal dominant associated with mutation in keratin 14 on chromosome 17. We report the case of a 31-year-old male presented with reticulate hyperpigmentation all over the body with diffuse noncicatricial alopecia and onychodystrophy of the finger and toe nails. He also had palmoplantar hypohydrosis and poorly developed dermatoglyphics. There were no other findings of ectodermal-derived organ involvement.
Databáze:	Directory of Open Access Journals
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