Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anisha P Bindagi"'
Autor:
Anisha P Bindagi, Sahana M Srinivas
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 24, Iss 2, Pp 157-160 (2023)
Universal acquired melanosis, also referred to as Carbon baby syndrome, is a rare cause of progressive generalized hyperpigmentation of skin and mucosa. We describe a case of a 2-year-old boy with diffuse darkening of skin and mucosa for 3 months of
Externí odkaz:
https://doaj.org/article/2c68782c4f0640f2a8954312b3499e75
Publikováno v:
Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 13, Iss 2, Pp 160-164 (2020)
BACKGROUND: Dermatophytosis is a common skin infection, having recurrent and persisting course because of topical steroid abuse, irregular treatment, and poor hygiene. The aim of this study was to assess the quality of life (QoL) of patients diagnose
Externí odkaz:
https://doaj.org/article/c9271f368e354857affdd6a611988596
Publikováno v:
Clinical Dermatology Review, Vol 5, Iss 2, Pp 223-225 (2021)
Porokeratosis (PK) is a rare group of heterogeneous disorders of keratinization representing diverse phenotypic expressions of the same genetic defect, which is mainly inherited in an autosomal dominant manner. This report describes the case of a 40-
Externí odkaz:
https://doaj.org/article/02bbb2571cf84f8696c0b5bffca69959
Publikováno v:
Indian Journal of Health Sciences and Biomedical Research KLEU, Vol 13, Iss 2, Pp 160-164 (2020)
BACKGROUND: Dermatophytosis is a common skin infection, having recurrent and persisting course because of topical steroid abuse, irregular treatment, and poor hygiene. The aim of this study was to assess the quality of life (QoL) of patients diagnose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad992dae28bda178951ae9fc165c336
http://www.ijournalhs.org/article.asp?issn=2542-6214
http://www.ijournalhs.org/article.asp?issn=2542-6214
Publikováno v:
Clinical Dermatology Review, Vol 5, Iss 2, Pp 223-225 (2021)
Porokeratosis (PK) is a rare group of heterogeneous disorders of keratinization representing diverse phenotypic expressions of the same genetic defect, which is mainly inherited in an autosomal dominant manner. This report describes the case of a 40-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b6203f3902bf73a27b27b769bb836c4
http://www.cdriadvlkn.org/article.asp?issn=2542-551X
http://www.cdriadvlkn.org/article.asp?issn=2542-551X