Results 41 to 50 of about 3,141 (175)

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

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

Acrodermatitis enteropática adquirida: reporte de un caso y revisión de la literatura

Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2019
La acrodermatitis enteropática es un raro trastorno producido por la deficiencia de cinc, que puede ser heredada o adquirida. Se caracteriza por la presencia de lesiones en la piel distribuidas en zonas distales o alrededor de orificios, alopecia y ...
Liliana Bohórquez, Cristina María Uribe, Ana Cristina Ruiz   +2 more
doaj  

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

Palmoplantar pustulosis: pathogenesis, differential diagnosis, and treatment

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 24, Issue 4, Page 516-535, April 2026.
Summary Palmoplantar pustulosis (PPP) is a chronic inflammatory and often painful disease characterized by sterile pustules on the palms and soles, significantly impairing quality of life. Women are more frequently affected than men, and smoking is a major trigger. Under biologic therapies, especially TNF antagonists, a paradoxical PPP may occur.
Rotraut Mössner, Tanja Fetter, Robert Sabat, Ulrich Mrowietz, Neda Cramer, Dagmar Wilsmann‐Theis   +5 more
wiley   +1 more source

Acrodermatitis Enteropathica

Medicine, 2016
Acrodermatitis enteropathica is a rare genetic autosomal recessive disorder, characterized by periorificial dermatitis, alopecia, and diarrhea. It is caused by mutations in the gene that encodes a membrane protein that binds zinc. We report a 14-month-old boy, admitted for erythematous, scaly and pustular lesions, initially located in the inguinal and ...
Nistor, Nicolai, Ciontu, Lavinia, Frasinariu, Otilia-Elena, Lupu, Vasile Valeriu, Ignat, Ancuta, Streanga, Violeta   +5 more
openaire   +2 more sources

Complications and Laboratory Test Findings Among Patients With Generalized Pustular Psoriasis: A Retrospective Chart Review Study

Experimental Dermatology, Volume 35, Issue 3, March 2026.
ABSTRACT Generalized pustular psoriasis (GPP) is a rare, chronic, inflammatory skin disease characterised by widespread eruption of sterile, macroscopic pustules. Patients with GPP can present with multiple comorbidities that may influence treatment. This study aimed to assess the frequency of psoriasis‐related complications and non–psoriasis‐related ...
Ryuhei Okuyama, Yukari Okubo, Shinichi Imafuku, Yayoi Tada, Keiichi Yamanaka, Kazumitsu Sugiura, Yukie Yamaguchi, Masahito Yasuda, Wataru Sakamoto, Morihisa Saitoh, Akimichi Morita   +10 more
wiley   +1 more source

Hereditary Acrodermatitis Enteropathica In Two Siblings

Indian Journal of Dermatology, 2003
Acrodermatitis enteropathica is a rare hereditary disorder of zinc metabolism characterized by dermatitis involving the acral and periorificial skin, diarrhea and growth retardation. Two siblings with classical features of acrodermatitis enteropathic and
Masood Quzi, Majid Imran
doaj  

Primary Cutaneous B‐Cell Lymphomas: An Updated Portrait of Classification, Biology, and Clinical Management

European Journal of Haematology, Volume 116, Issue 2, Page 116-128, February 2026.
ABSTRACT Primary cutaneous B‐cell lymphomas (CBCL) represent a clinically and biologically heterogeneous group of extranodal non‐Hodgkin lymphomas confined to the skin at the time of diagnosis. They account for approximately 25% of all primary cutaneous lymphomas and are subclassified into distinct entities according to the World Health Organization ...
A. Bernardelli, E. Carazzai, B. Bugnotto, F. Bellinato, M. Krampera, C. Visco   +5 more
wiley   +1 more source

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