Results 51 to 60 of about 2,564 (144)

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 Eruptions in a Child with Hartnup Disease

, 2006
Acrodermatitis enteropathica-like eruptions, not related to zinc deficiency, have been rarely reported in some metabolic disorders. Reported patients usually had low levels of essential amino acids, particularly isoleucine.
Sevin Altınkaynak, Selimoglu, Mukadder Ayse, Osman Fidanoğlu, Mukadder Ayşe Selimoğlu, Muammer Eşrefoğlu Seyhan, Vildan Ertekin, Fidanoglu, Osman, Altinkaynak, Sevin, Ertekin, Vildan, Seyhan, Muammer Esrefoglu   +9 more
core   +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

A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient With A Novel Mutation In Slc39A4 Gene [PDF]

, 2011
Acrodermatitis enteropathica (AE) is a rare autosomal recessive disorder of zinc deficiency due to an abnormal intestinal zinc transporter. It is characterized by the triad of acral dermatitis, alopecia, and diarrhoea.
Kilic, M., M. Taskesen, Tokatlı, A., Sivri, H. S., F. Gürakan, Tokatli, A., Dursun, A., S. Schmitt, M. Kilic, DURSUN, ALİ, Tokatli, AYŞEGÜL, S. Küry, Schmitt, S., A. Tokatli, A. Dursun, Kury, S., Taskesen, M., Gurakan, F., Coskun, T., T. Coskun, Kılıc, M., H. S. Sivri   +21 more
core   +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

Acrodermatitis enteropathica: Shedding the light on an under-recognised nutritional disorder

Proceedings of Singapore Healthcare
Acrodermatitis enteropathica is an uncommon nutritional disorder caused by zinc deficiency, characterised by the triad of periorificial dermatitis, alopecia and diarrhoea.
Chee Hoou Loh, Adeline Lam Ee Ling, Yee Kiat Heng   +2 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

Hereditary acrodermatitis enteropathica: A case report

Pifu-xingbing zhenliaoxue zazhi
We report a case of hereditary acrodermatitis enteropathica. A 12-year old boy was admitted to the hospital due to recurrent skin erythema around the mouth and buttocks for 12 years and aggravation for 2 months.
LI Jibing, CHEN Guanghua, JIANG Jinqiu, LI Hongmei, QIAN Hua, LUO Xiaoyan   +5 more
doaj   +1 more source

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

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