Results 21 to 30 of about 11,602 (301)

Acrodermatitis Atrophicans Herxheimer [PDF]

Proceedings of the Royal Society of Medicine, 1935
Hugh Gordon
openalex   +3 more sources

A clinical case of familial enteropathic acrodermatitis caused by a new genetic mutation in exon 10 of the SLC39A4 gene [PDF]

Alʹmanah Kliničeskoj Mediciny, 2021
Enteropathic acrodermatitis is a rare form of genodermatoses, a group of hereditary disorders with prevailing skin lesions. The disease manifestation in children is associated with withdrawal of breastfeeding and switch to the cow milk-based products ...
Antonina S. Stadnikova, Olga B. Tamrazova, Irina N. Zakharova, Yulia A. Dmitrieva, Alexey V. Taganov, Anastasiya E. Yudina, Gayane E. Bagramova   +6 more
doaj   +1 more source

Acrodermatitis continua of Hallopeau and generalised pustular psoriasis: Should they be the same or different entities?

Experimental Dermatology, 2023
Pustular psoriasis is characterised by eruptions of neutrophilic sterile pustules. The European Rare and Severe Psoriasis Expert Network consensus defines pustular psoriasis into three subtypes; generalised pustular psoriasis (GPP), palmoplantar ...
L. Chularojanamontri, Krittaya Rattanakorn, N. Julanon, M. Chuamanochan, C. Griffiths   +4 more
semanticscholar   +1 more source

Acrodermatitis Enteropathica: A Rare Case With Lifelong Implications

Cureus, 2023
Acrodermatitis enteropathica is a rare genetic disorder caused by a defect in intestinal zinc absorption, resulting in zinc deficiency and various clinical manifestations, including dermatitis, diarrhea, alopecia, and nail abnormalities.
Muhannad M Alwadany, Abdullah F Al Wadani, F. Almarri, Hadi S Alyami, Muhammad A Al-Subaie   +4 more
semanticscholar   +1 more source

A case of recurrent vaccine-triggered Gianotti–Crosti syndrome

Future Science OA, 2021
Gianotti–Crosti syndrome (GCS) is a self-limited benign dermatosis, clinically characterized by a monomorphic papular or papulovesicular eruption symmetrically distributed on the limbs and face of children.
Joy Assaf, Farid Stephan, P Zeinaty, Roland Tomb   +3 more
doaj   +1 more source

Acrodermatitis chronica atrophicans: clinical and microbiological characteristics of a cohort of 693 Slovenian patients

Journal of Internal Medicine, 2021
Information on large groups of patients with acrodermatitis chronica atrophicans (ACA) is limited.
K. Ogrinc, V. Maraspin, L. Lusa, T. Cerar Kišek, E. Ružić-Sabljić, F. Strle   +5 more
semanticscholar   +1 more source

Clinical Images: Local bone loss in a patient with acrodermatitis continua of Hallopeau [PDF]

ACR Open Rheumatol
ACR Open Rheumatology, Volume 8, Issue 2, February 2026.
Bellinato F, Gisondi P, Girolomoni G, Rossini M, Viapiana O, Adami G.   +5 more
europepmc   +2 more sources

Zinc transporter mutations linked to acrodermatitis enteropathica disrupt function and cause mistrafficking

Journal of Biological Chemistry, 2021
ZIP4 is a representative member of the Zrt-/Irt-like protein (ZIP) transporter family and responsible for zinc uptake from diet. Loss-of-function mutations of human ZIP4 (hZIP4) drastically reduce zinc absorption, causing a life-threatening autosomal ...
Eziz Kuliyev, Chi Zhang, D. Sui, Jian Hu
semanticscholar   +1 more source

Acrodermatitis Continua of Hallopeau Evolving into Generalized Pustular Psoriasis Following COVID‐19: A Case Report of a Successful Treatment with Infliximab in Combination with Acitretin

Biologics : targets & therapy, 2021
The global pandemic of coronavirus disease 2019 (COVID-19) caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is emerging.
Dominik Samotij, Ewelina Gawron, Justyna Szczęch, Elżbieta Ostańska, A. Reich   +4 more
semanticscholar   +1 more source

Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis. [PDF]

Cureus
Alsulami EA, Alghamdi MS, Alraddadi AE, Alabbasi AK, Allehaibi LZ, Al Hawsawi W, Al Hawsawi K.   +6 more
europepmc   +3 more sources