Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Fares A. Alkhayal"'
Publikováno v:
Skin Health and Disease, Vol 4, Iss 3, Pp n/a-n/a (2024)
Abstract Aquagenic keratoderma, also known as aquagenic wrinkling of the palms, transient reactive papulotranslucent acrokeratoderma, or transient aquagenic hyper‐wrinkling, is an uncommon disorder that affects the palms and occasionally the soles.
Externí odkaz:
https://doaj.org/article/10434e74838c4cf2a12c616ea7d9d357
Publikováno v:
Dermatology Reports (2023)
Acrodermatitis dysmetabolica (AD) describes eruptions characterized by the clinical triad of acral dermatitis, diarrhea, and alopecia. AD can be caused by various metabolic disorders one of which is maple syrup urine disease (MSUD). We present a 2-mo
Externí odkaz:
https://doaj.org/article/9e74ef538f4a4656bf6b3ebd458c50f0
Publikováno v:
Dermatology Reports (2023)
Keratosis pilaris (KP) is a common disorder of follicular keratinization characterized by keratotic follicular papules with varying degrees of perifollicular erythema. Keratosis pilaris affects up to half of normal children and up to three-quarters o
Externí odkaz:
https://doaj.org/article/dff47e085c49439880b2f100a34799f4
Publikováno v:
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous pap
Externí odkaz:
https://doaj.org/article/8d61a89e86a54ef089996f3135fa1334
Publikováno v:
Case Reports in Oncology, Vol 11, Iss 2, Pp 436-441 (2018)
The Leser-Trélat sign is a rare sign of some malignant tumors and is characterized by the sudden appearance of seborrheic keratosis in association with an underlying malignancy. We describe a 60-year-old Saudi man with mycosis fungoides (MF) who dev
Externí odkaz:
https://doaj.org/article/6e4f46388241405e928fe73a738d4db2
Keratosis pilaris (KP) is a common disorder of follicular keratinization characterized by keratotic follicular papules with varying degrees of perifollicular erythema. Keratosis pilaris affects up to half of normal children and up to three-quarters o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::071d22c4d619475d4fdb7f267d4b07e8
https://doi.org/10.22541/au.165726024.47685537/v1
https://doi.org/10.22541/au.165726024.47685537/v1
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Clinical Case Reports, Vol 9, Iss 9, Pp n/a-n/a (2021)
Graham‐Little Piccardi Lassueur Syndrome (GLPLS) is a rare variant of lichen planopilaris (LPP) which characterized by triad of fibrosing alopecia of the scalp, non‐fibrosing alopecia of the axilla and groin, and a follicular spinous papule over
Publikováno v:
Case Reports in Oncology
Case Reports in Oncology, Vol 11, Iss 2, Pp 436-441 (2018)
Case Reports in Oncology, Vol 11, Iss 2, Pp 436-441 (2018)
The Leser-Trélat sign is a rare sign of some malignant tumors and is characterized by the sudden appearance of seborrheic keratosis in association with an underlying malignancy. We describe a 60-year-old Saudi man with mycosis fungoides (MF) who dev
Autor:
AlKhayal, Fares A1 (AUTHOR) falkhayal@outlook.com, Albusair, Moath K1 (AUTHOR)
Publikováno v:
Oxford Medical Case Reports. Mar2024, Vol. 2024 Issue 3, p1-3. 3p.
Publikováno v:
Skin Health & Disease; Jun2024, Vol. 4 Issue 3, p1-4, 4p