Results 131 to 140 of about 4,685 (212)

Cobblestone appearance of oral mucosa: A diagnostic conundrum. [PDF]

SAGE Open Med Case Rep
Gowda SK, Dhakad R, Jain S, Sethuraman G.   +3 more
europepmc   +1 more source

Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in <i>FAM83G</i>. [PDF]

Front Med (Lausanne)
Mora-Gómez M, Feito M, Gallego-Zazo N, Maseda-Pedrero R, Sobral-Costas TG, Miranda-Alcaraz L, Vásquez-Amell V, Rodríguez-Canó M, Parra A, Cazalla M, Arias P, Silván C, Jiménez-Estrada JA, Ruiz-Pérez VL, Nevado J, Lapunzina P, Tenorio-Castano J.   +16 more
europepmc   +1 more source

Effective Management of Familial Erythrokeratoderma Using Topical Calcipotriol. [PDF]

Cureus
Kulandaivelavan T, Harikumar MV, Dennis Joseph L, Swaminathan A.   +3 more
europepmc   +1 more source

Huriez Syndrome. [PDF]

Indian Dermatol Online J
Singh S, Das S.
europepmc   +1 more source

Sporadic Case of Acrokeratosis Verruciformis of Hopf With Unusual Clinical Presentation: A Case Report and Review of the Literature. [PDF]

Cureus
Cabello-Hernández AI, Rodríguez-Rangel X, Polanco-Llanes AS, Toussaint-Caire S, Domínguez-Cherit J.   +4 more
europepmc   +1 more source

Multiple Cutaneous Squamous Cell Carcinomas on Primary Epidermodysplasia Verruciformis in a 19-Year-Old Black Subject. [PDF]

Case Rep Dermatol Med
Kassang P, Mouhari-Toure A, Djiwa T, Akakpo SA, Teclessou JN, Saka B, Pitche P.   +6 more
europepmc   +1 more source

Association of erlotinib and acitretin for the treatment of Olmsted syndrome with erythromelalgia in a pediatric patient. [PDF]

An Bras Dermatol
Azulay-Abulafia L, Rodrigues Fagundes J, Ollague Cordova EE, Diniz Pacheco K, Hovnanian A.   +4 more
europepmc   +1 more source

A rare presentation of dyschromatosis symmetrica hereditaria in a Canadian context: A case report. [PDF]

SAGE Open Med Case Rep
Czyz S, Jafarian F, Holfeld K.
europepmc   +1 more source

Kindler Syndrome in a 24-Year-Old Male: A Clinical Diagnosis in the Absence of Genetic Testing: A Rare Case Report. [PDF]

Case Rep Dermatol Med
Ahmad DS, Nasser R, Mahmoud A, Al-Janabi MH, Al-Shehabi Z, Hassan F.   +5 more
europepmc   +1 more source

Vitamin B12 deficiency secondary to cobalamin F deficiency simulating dyskeratosis congenita

JAAD Case Reports, 2020
Lama Altawil, MD, Hind Alshihry, MD, Hala Ahmed, MD, Hanan E. Shamseldin, MD, Fowzan Alkuraya, MD   +4 more
doaj   +1 more source