Results 31 to 40 of about 3,141 (175)

Acrodermatitis enteropathica, a discussion and report of a case successfully treated

The Turkish Journal of Pediatrics, 1959
A brief discussion of acrodermatitis enteropathica has been presented with a case report of an infant with typical findings of this disease who was recently admitted to the Hacettepe Children's Hospital.
Joe D. Wray, Altan Günalp, Münevver Bertan   +2 more
doaj   +1 more source

Lesões de pele do tipo acrodermatite enteropática em duas crianças com doença da urina de xarope do bordo Acrodermatitis enteropathica-like eruption in two children with maple syrup urine disease

Anais Brasileiros de Dermatologia, 2007
Lesões cutâneas semelhantes à acrodermatite enteropática têm sido descritas em pacientes com algumas doenças metabólicas tratadas com dietas hipoprotéicas.
Erasmo Barbante Casella, Maria Esther Jurfest Rivero, Maria Rosa Machado Mercado, Maria Aparecida Vieira, Maria Joaquina Marques-Dias, Flávio Adolfo Costa Vaz   +5 more
doaj   +1 more source

Acrodermatitis continua of Hallopeau with psoriatic arthritis treated with biologics and apremilast

JEADV Clinical Practice, 2023
Acrodermatitis continua of Hallopeau (ACH) is a rare variant of acral pustular psoriasis, exclusively involving the distal phalanges and nails of the hands and feet.
Shohei Igari, Toshiyuki Yamamoto
doaj   +1 more source

Prurigo Pigmentosa – an increasingly diagnosed dermatological condition associated with ketogenic diet

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
SUMMARY Prurigo pigmentosa (PP) is a rare inflammatory dermatosis, clinically characterized by intensely pruritic, erythematous papules and papulovesicles, with reticular hyperpigmentation upon healing. We herein report four cases in adults of different ethnic backgrounds, in which the disease was associated with ketogenic metabolic states due to ...
Antigona Aliu, Milan Vidakovic, Marcel Krauß, Julia Hyun, Frank Oellig, Thilo Gambichler, Valentina Laura Müller, Alexander Kreuter   +7 more
wiley   +1 more source

Male genital lichen sclerosus

Journal of the European Academy of Dermatology and Venereology, EarlyView.
Male genital lichen sclerosus is driven by chronic, occluded exposure of susceptible genital epithelium to urine, rather than infection or autoimmunity. This review synthesizes clinical, anatomical and molecular evidence showing how microincontinence and occlusion initiate inflammation, fibrosis and carcinogenesis, and explains the curative effect of ...
Georgios Kravvas, Rory Barry, Richard E. Watchorn, Christopher B. Bunker   +3 more
wiley   +1 more source

Multiple Carboxylase Deficiency in an Infant Presenting With Severe Metabolic Acidosis and Sepsis‐Like Features: A Case Report and Literature Review

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Multiple carboxylase deficiency (MCD) is a rare, treatable inborn error of biotin metabolism that may present in children in the first year of life with life‐threatening metabolic crises. We report a 4‐month‐old child presenting with persistent seizures, eczematous rash near the orifices, unjustified loss of hair with baldness, and severe ...
Touqeer Rehman, Riyan Saeed, Muhammad Ahmed Akif Rauf, Luqman Asif, Muhammad Junaid, Muddassir Khalid, Rao Nouman Ali, Umair Ali, Fred Segawa   +8 more
wiley   +1 more source

European S2k guidelines on management of autoimmune blistering diseases in children and adolescents

Journal of the European Academy of Dermatology and Venereology, Volume 40, Issue 7, Page 1137-1161, July 2026.
Autoimmune blistering disorders (AIBDs) in children are rare, challenging to diagnose and treat and often require immunosuppressants. Until now, no paediatric care guidelines existed. The EADV Task Force for AIBDs has developed the consensus‐based recommendations, enabling physicians to adopt a uniform, tailored treatment strategy to improve outcomes ...
A. Nanda, B. Tedbirt, C. Bodemer, M. C. Bolling, M. El Hachem, M. Nikolić, E. Benton, M. Caproni, D. De, D. Didona, K. Drenovska, M. Goebeler, M. Hertl, B. Horváth, M. Kasperkiewicz, D. Kiritsi, M. Larralde, A. V. Marzano, J. Meijer, D. F. Murrell, J. Powell, E. Sprecher, N. S. Chandran, M. M. Tomayko, S. Uzun, N. van Beek, H. Ott, A. Patsatsi, A. Torrelo, A. Welfringer‐Morin, E. Schmidt, P. Joly   +31 more
wiley   +1 more source

Clinical analysis of 20 cases of childhood acrodermatitis enteropathica

Pifu-xingbing zhenliaoxue zazhi
Objective To investigate the clinical features of acrodermatitis enteropathica (AE). Methods A retrospective analysis was conducted on the clinical data of 20 children diagnosed with acrodermatitis enteropathica in the outpatient clinic at the ...
Jibing LI, Wei LI, Cui HU, Yingying QIAN, Ting ZHANG, Yafen WU, Hua QIAN   +6 more
doaj   +1 more source

An Acrodermatitis Enteropathica Case

Van Tıp Dergisi, 2019
Acrodermatitis enteropathica is a rare autosomal recessive inherited disease resulting in zinc deficiency. As a result of disrupted intestinal absorption of zinc, zinc deficiency occurs. Periorificial dermatitis, diarrhea, alopecia and growth retardation
Sevda Önder, Havva Erdem, Göktürk Dere   +2 more
doaj   +1 more source

Acrodermatitis Enteropathica: A Case Report

Oman Medical Journal, 2020
Acrodermatitis enteropathica is a rare autosomal recessive disease caused by a genetic mutation leading to zinc deficiency. Clinical manifestation includes skin lesions, diarrhea, and alopecia.
Asma Al Naamani, Tuqa Al Lawati
doaj   +1 more source