Results 11 to 20 of about 5,847 (202)

Acrodermatitis enteropathica-like eruption [PDF]

open access: yesJAAD Case Reports, 2022
Farah El Hadadi, MD   +4 more
doaj   +4 more sources

Acrodermatitis Enteropathica

open access: yesJAMA Dermatology, 2023
This case report describes a woman in her 20s with painful, red skin lesions present for 6 months that had gradually progressed from the groin to other sites.
Jagadeesan S, Kaliyadan F.
europepmc   +4 more sources

Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature [PDF]

open access: yesBMC Pediatrics, 2020
Background Acrodermatitis enteropathica (AE) is a rare autosomal recessive hereditary skin disease caused by mutations in the SLC39A4 gene and is characterized by periorificial dermatitis, alopecia and diarrhoea due to insufficient zinc absorption.
Wei Zhong   +4 more
doaj   +3 more sources

Acquired acrodermatitis enteropathica from a ketogenic diet [PDF]

open access: yesJAAD Case Reports, 2021
Sabah Osmani, BA   +3 more
doaj   +3 more sources

Acrodermatitis dysmetabolica with concomitant acquired acrodermatitis enteropathica in a patient with maple syrup urine disease [PDF]

open access: yesJAAD Case Reports
Luis E. Santaliz-Ruiz, IV, MD   +3 more
doaj   +3 more sources

A case of acrodermatitis enteropathica

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2022
Acrodermatitis enteropathica (AE) is a rare genetic autosomal recessive disorder of zinc deficiency which manifests in infancy with triad of peri-orificial skin rash, alopecia, and diarrhea. We report the case of an 8-month-old infant with dermatological
Pankaj Das   +5 more
doaj   +2 more sources

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

open access: yesProceedings 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   +2 more
doaj   +2 more sources

A mouse model of acrodermatitis enteropathica: loss of intestine zinc transporter ZIP4 (Slc39a4) disrupts the stem cell niche and intestine integrity. [PDF]

open access: yesPLoS Genetics, 2012
Mutations in the human Zip4 gene cause acrodermatitis enteropathica, a rare, pseudo-dominant, lethal genetic disorder. We created a tamoxifen-inducible, enterocyte-specific knockout of this gene in mice which mimics this human disorder. We found that the
Jim Geiser   +3 more
doaj   +6 more sources

A novel case of limbal stem cell deficiency in a patient with acrodermatitis enteropathica

open access: yesOman Journal of Ophthalmology, 2023
An 18-year-old male diagnosed with acrodermatitis enteropathica (AE) since early childhood presented with worsening of dermatitis along with photophobia and watering in both eyes.
Gayatri Sundareswaran   +2 more
doaj   +2 more sources

Variants of SLC39A4 cause acrodermatitis enteropathica in Tibetan, Yi, and Han families in Sichuan region of southwestern China: a case report series [PDF]

open access: yesFrontiers in Medicine
Acrodermatitis enteropathica (AE, OMIM 201100) is a rare autosomal recessive dermatosis characterized by periorificial dermatitis, diarrhea, alopecia, and hypozincaemia due to pathogenic variants of SLC39A4.
Zhongtao Li   +3 more
doaj   +2 more sources

Home - About - Disclaimer - Privacy