Results 61 to 70 of about 2,564 (144)
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
A 4-month-old boy with acrodermatitis enteropathica-like symptoms
, 2009 A 4-month-old boy was admitted for having diffuse eruption in the perianal region, legs, trunk hands, and face with failure to thrive, edema, hypoalbuminemia, and anemia.
Çobanoğlu, Nazan
core +2 more sources
Erkennen – Der klinische Blick auf die kutane Tuberkulose
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 7, Page 793-803, July 2025.Zusammenfassung In vielen Ländern ist die Tuberkulose (TBC) bis heute eine der häufigsten Todesursachen und bleibt insbesondere durch Migrationsbewegungen auch in Deutschland von Bedeutung. Die Diagnose der seltenen kutanen Tuberkulose ist herausfordernd, da sie in vielfältigen klinischen Erscheinungsformen auftritt, die deutlich häufigeren ...
Cathrin Gramminger, Tilo Biedermann
wiley +1 more source
Characteristics of the cases of acrodermatitis Enteropathica accompanied by metabolic diseases
The detailed information of the literature we reviewed in this study-Acrodermatitis Enteropathica in pediatrics: Zinc is not the whole.There were 80 cases and 52 references, all of which were case reports or case series of AE with metabolic ...
Sun, Yuming
core +4 more sources
A rare case of familial methylmalonic acidemia presenting with Acrodermatitis Enteropathica type of lesion [PDF]
, 2017 Methylmalonic academia (MMA) is an inborn error of metabolism commonly presenting in newborns with an occurrence of 1 in 50,000 to 80,000 newborns. It has autosomal recessive mode of inheritance. It is a disorder of amino acid metabolism.
P. Wali, Pradnya +2 more
core +1 more source
United European Gastroenterology Journal, Volume 13, Issue 5, Page 773-797, June 2025.ABSTRACT Malabsorption is a complex and multifaceted condition characterised by the defective passage of nutrients into the blood and lymphatic streams. Several congenital or acquired disorders may cause either selective or global malabsorption in both children and adults, such as cystic fibrosis, exocrine pancreatic insufficiency (EPI), coeliac ...
Marco Vincenzo Lenti +29 more
wiley +1 more source
Acrodermatitis enteropathica: the need for sustained high dose zinc supplementation [PDF]
, 2018 Acrodermatitis enteropathica (AE) is a rare congenital disorder owing to an abnormality with intestinal absorption and/or transportation of zinc. We describe two male siblings, who presented with evidence of both acute and chronic zinc deficiency ...
Ranugha, PSS +2 more
core +1 more source
Acrodermatitis enteropathica in pediatrics: Zinc is not the whole
The detailed information of the literature we reviewed in this study-Acrodermatitis Enteropathica in pediatrics: Zinc is not the whole.
Sun, Yuming
core +2 more sources
An 11‐Month‐Old Infant With Unusual Diaper Dermatitis
JEADV Clinical Practice, Volume 5, Issue 2, Page 731-733, June 2026.
Majda Chaoui +2 more
wiley +1 more source
The Intestinal Transporter SLC30A1 Plays a Critical Role in Regulating Systemic Zinc Homeostasis
Advanced Science, Volume 11, Issue 46, December 11, 2024.Intestinal SLC30A1 plays an essential role for controlling systemic zinc homeostasis via its basolateral membrane‐localized transporter activity of zinc ions from intestinal epithelial cells (IECs) to the circulation. The lethal phenotype of intestinal Slc30a1 deficient mice can be fully rescued by systemic zinc supplementation.
Shumin Sun +16 more
wiley +1 more source