Results 41 to 50 of about 1,437 (155)

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 variants of acrodermatitis enteropathica and its co-relation with genetics

Indian Journal of Paediatric Dermatology, 2016
Acrodermatitis enteropathica (AE) is a rare disorder of zinc deficiency, which manifests as acral and periorificial dermatitis, alopecia, intractable diarrhea, and failure to thrive.
Sarabjit Kaur, Ankita Sangwan, Priyadarshini Sahu, Surabhi Dayal, Vijay Kumar Jain   +4 more
doaj   +1 more source

Transient zinc deficiency syndrome in a breast-fed infant due to decreased zinc in breast milk (type II hypozincemia of infancy): A case report and review of the literature

Dermatologica Sinica, 2012
Type II hypozincemia of infancy is a rare, hereditary zinc deficiency occurring in infants while exclusively on breast feeding. It is caused by defective transfer of zinc into breast milk. Only a few dozen cases have been reported.
Wei-Li Yang, Chao-Kai Hsu, Sheau-Chiou Chao, Ching-Yuang Huang, Julia Yu-Yun Lee   +4 more
doaj   +1 more source

Nutritional Deficiencies Following Bariatric Surgery: A Rapid Systematic Review of Case Reports of Vitamin and Micronutrient Deficiencies Presenting More Than Two Years Post‐Surgery

Clinical Obesity, Volume 15, Issue 6, December 2025.
ABSTRACT Bariatric surgery is the most clinically‐ and cost‐effective intervention for severe obesity. However, without adequate follow‐up, it can lead to nutritional deficiencies. Patients require life‐long nutritional supplements and follow‐up to prevent nutritional deficiencies from developing.
Sophie Haughton, Sarah Gentry, Helen M. Parretti   +2 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  

Atypical presentation of cystic fibrosis in an infant

Journal of Pediatric Critical Care, 2018
Dermatopathy as an initial manifestation of cystic fibrosis (CF) in the newborn period is unusual. The eruption is usually first noted in the perineum, typically appears in infancy from age 2 weeks to 15 months after birth. It subsequently spreads to the
Bandya Sahoo, Mukesh Kumar Jain, Reshmi Mishra, Sibabratta Patnaik   +3 more
doaj   +1 more source

Micronutrient deficiencies after pancreatico‐duodenectomy: A narrative review of the literature and recommendations for clinical practice

Nutrition in Clinical Practice, Volume 40, Issue 5, Page 1073-1092, October 2025.
Abstract Micronutrient uptake is impaired after pancreatico‐duodenectomy (PD) because of malabsorption, reduced absorptive capacity, and poor oral intake. Biochemical depletion is reported in cohort studies, but deficiency states are predominantly reported in case reports, making it difficult to assess occurrence rates.
Mary E. Phillips, Callum Livingstone, Adam E. Frampton, Kathryn H. Hart   +3 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

Dental considerations in acrodermatitis enteropathica: A report of two cases [PDF]

Journal of Oral Health and Oral Epidemiology, 2019
BACKGROUND AND AIM: Acrodermatitis enteropathica (AE) is a rare and severe genetic disorder with autosomal recessive inheritance, which is usually diagnosed with deficiency of zinc intestinal absorption.
Mahboobeh Shokrizadeh, Fatemeh Sadat Sajadi   +1 more
doaj   +1 more source

Recognising cutaneous tuberculosis

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 793-802, July 2025.
Summary Tuberculosis (TB) continues to be a leading cause of death in many countries, and also remains a significant concern in Germany, particularly due to migration. The diagnosis of rare cutaneous tuberculosis is challenging as it manifests in various clinical forms that resemble more common dermatological conditions.
Cathrin Gramminger, Tilo Biedermann
wiley   +1 more source