Results 71 to 80 of about 11,602 (301)

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

Journal of the European Academy of Dermatology and Venereology, EarlyView.
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

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

A genome-wide search for risk genes using homozygosity mapping and microarrays with 1,494 single-nucleotide polymorphisms in 22 eastern Cuban families with bipolar disorder [PDF]

, 2005
Homozygosity mapping is a very powerful method for finding rare recessive disease genes in monogenic disorders and may also be useful for locating risk genes in complex disorders, late onset disorders where parents often are not available, and for rare ...
American Psychiatric Association, Baron, Bennett, Bull, Bull, Curtis, Dick, Ewald, Ewald, Houwen, Kruglyak, Kruglyak, Lander, Miano, Modin, Primdahl, Segurado, van Duijn, Wang, Wing, World Health Organization, Wright   +21 more
core   +1 more source

Biologic therapy for acrodermatitis continua of Hallopeau: Successful treatment with secukinumab and review of the literature

Dermatologic Therapy, 2019
Acrodermatitis continua of Hallopeau (ACH) is a rare pustular psoriasis variant refractory to many conventional treatments. We report the successful treatment with secukinumab of a patient with a long history of ACH with marked onychodystrophy with frank
M. Galluzzo, S. D’adamio, M. Teoli, L. Bianchi, M. Talamonti   +4 more
semanticscholar   +1 more source

Dermatologic Findings of RELA‐Associated Autoinflammatory Disease

Pediatric Dermatology, EarlyView.
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

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

Topical tacrolimus 0.1% ointment for treatment of cutaneous Crohn's Disease [PDF]

, 2013
Peer reviewedPublisher ...
El-Omar, Emad, Keenan, Ronald A, Ormerod, Anthony D, Rice, Shantini A, Woo, Pick N   +4 more
core   +2 more sources

Acrodermatitis enteropathica

British Journal of Dermatology, 1979
The first publication identifying acrodermatitis enteropathica as a definite disease (Danbolt & Closs, 1942) is reviewed. Later studies are briefly surveyed, resulting in the recognition of the disease as a zinc deficiency which can be effectively corrected by administration of small oral doses of zinc.
openaire   +4 more sources

Palmoplantare Pustulose: Entstehung, Differentialdiagnose und Therapie

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 516-536, April 2026.
Zusammenfassung Die palmoplantare Pustulose (PPP) ist eine chronisch entzündliche, häufig schmerzhafte Erkrankung mit sterilen Pusteln an Handflächen und Fußsohlen, die die Lebensqualität stark einschränkt. Frauen sind häufiger betroffen als Männer, und Rauchen ist ein bedeutender Provokationsfaktor.
Rotraut Mössner, Tanja Fetter, Robert Sabat, Ulrich Mrowietz, Neda Cramer, Dagmar Wilsmann‐Theis   +5 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