Results 41 to 50 of about 4,377 (156)

Borrelia and Genital Lichen Sclerosus: A Critical Review of the Evidence

JEADV Clinical Practice, Volume 5, Issue 3, Page 777-785, September 2026.
We reviewed the evidence linking Borrelia as an aetiological factor to LSc. Thirty‐six studies were included. No significant differences in Borrelia detection were observed between LSc and comparator dermatoses using ELISA, PCR, culture, or microscopy. A significant difference observed with IHC was considered an outlier.
Liang Zhi Wong, Richard Watchorn, Sandra Jerkovic Gulin, Christopher B. Bunker, Georgios Kravvas   +4 more
wiley   +1 more source

Bullous acrodermatitis enteropathica: case report of a unique clinical presentation and review of the literature [PDF]

, 2015
Acrodermatitis enteropathica is a rare autosomal recessive disease characterized by pink scaly plaques and erosions in the periorificial and acral regions.
Chambers, Cindy, Iyengar, Sanjana, Sharon, Victoria R   +2 more
core   +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

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

Acrodermatitis chronica atrophicans.

, 1988
Two cases of acrodermatitis chronica atrophicans associated with Borrelia burgdorferi infection are reported; to our knowledge these are the first cases reported in ...
Flueler U, Boltshauser E, Gundelfinger R, Nadal D   +3 more
core   +1 more source

A case of acrodermatitis enteropathica

, 2000
Acrodermatitis enteropathica is a rare hereditary disorder affecting zinc metabolism that is characterized by dermatitis, alopecia, gastrointestinal disturbances, eye infections, and growth failure.
Ozturkcan S., Akyol M., Icagasioglu D., Cevit O.   +3 more
core   +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

[Acrodermatitis enteropathica-like skin lesions due to Crohn's disease-associated zinc deficiency] [PDF]

, 2010
We report a case of acrodermatitis enteropathica-like skin eruptions presenting with alopecia, perlèche, glossitis, and genital erosions as well as multifocal eczematoid, psoriasiform, and bullous skin lesions due to zinc deficiency in Crohn's ...
V. von Felbert, Hunziker, Thomas, T. Hunziker, von Felbert, V, Hunziker, T, von Felbert, Verena   +5 more
core   +2 more sources

Cow’s Milk Protein Allergy Mimicking Acrodermatitis Enteropathica [PDF]

Journal of Clinical and Diagnostic Research, 2014
Cow’s milk protein allergy is an adverse immune reaction to one or more of the constituent proteins of milk obtained from any animal, most commonly alpha s 1-casein cow’s milk. In many cases, the allergy is genetic in origin.
John Solomon, Rugmini Kamalammal, Mohammed Yaseen Sait, Harita Lohith   +3 more
doaj   +1 more source

Dermatologic Findings of RELA‐Associated Autoinflammatory Disease

Pediatric Dermatology, Volume 43, Issue 4, Page 925-928, July/August 2026.
ABSTRACT Variants in the gene RELA have been implicated in a monogenic, hereditary form of Behcet's‐like syndrome. This case series describes the dermatologic manifestations of three patients with identified RELA‐associated autoinflammatory disease.
Elizabeth Nourse, Vidya Sivaraman, Catherine G. Chung, Shoghik Akoghlanian, Esteban Fernandez Faith   +4 more
wiley   +1 more source