Results 91 to 100 of about 5,847 (202)

Hereditary acrodermatitis enteropathica: A case report

open access: yesPifu-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   +5 more
doaj   +1 more source

European Consensus on Malabsorption—UEG & SIGE, LGA, SPG, SRGH, CGS, ESPCG, EAGEN, ESPEN, and ESPGHAN

open access: yesUnited 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

Atypical presentation of cystic fibrosis in an infant

open access: yesJournal 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   +3 more
doaj   +1 more source

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

open access: yesJournal 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   +1 more
doaj   +1 more source

Development of Bullous Acrodermatitis Enteropathica during the Course of Chemotherapy for Acute Lymphocytic Leukemia [PDF]

open access: yes, 2011
Acrodermatitis enteropathica (AE) is an uncommon autosomal recessive genetic disorder of zinc malabsorption. The acquired form may be associated with inadequate intake, impaired absorption, and increased excretion of zinc.
Baik Kee Cho   +18 more
core   +3 more sources

Topical tacrolimus 0.1% ointment for treatment of cutaneous Crohn's Disease [PDF]

open access: yes, 2013
Peer reviewedPublisher ...
El-Omar, Emad   +4 more
core   +2 more sources

An 11‐Month‐Old Infant With Unusual Diaper Dermatitis

open access: yes
JEADV Clinical Practice, EarlyView.
Majda Chaoui   +2 more
wiley   +1 more source

The Intestinal Transporter SLC30A1 Plays a Critical Role in Regulating Systemic Zinc Homeostasis

open access: yesAdvanced 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

Investigation of chronic diarrhoea in infancy. [PDF]

open access: yes, 2013
Diarrhoea in infants and young children is defined as >200g/day of stools, and occurs when there is an imbalance between intestinal fluids absorption and secretion.
BERNI CANANI, Roberto   +5 more
core   +1 more source

A comprehensive investigation of biochemical status in patients with telogen effluvium: Analysis of Hb, ferritin, vitamin B12, vitamin D, thyroid function tests, zinc, copper, biotin, and selenium levels

open access: yesJournal of Cosmetic Dermatology, Volume 23, Issue 12, Page 4277-4284, December 2024.
Abstract Aim The etiology of telogen effluvium (TE) includes situations that may cause physiological stress, surgical trauma, inflammatory, infectious, iatrogenic causes, medications and nutritional deficiencies. TE has been associated with iron deficiency, vitamin B12 deficiency and thyroid diseases.
Irem Nur Durusu Turkoglu   +4 more
wiley   +1 more source

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