Results 11 to 20 of about 2,694 (199)

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

Oman 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, Neha Arora, Anandan Sankarasubramaniam   +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]

Frontiers 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, Zhongtao Li, Sheng Wang, Sheng Wang   +3 more
doaj   +2 more sources

Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock [PDF]

BMC Pediatrics
Background Acrodermatitis enteropathica (AE) is a rare autosomal recessive condition caused by mutations in the SLC39A4 gene, leading to a zinc absorption disorder. The hallmark features of AE are periorificial erosive dermatitis, hair loss, and diarrhea.
Elaheh Foroughi, Bahareh Abtahi-Naeini, Maryam Derakhshan, Noushin Rostampour, Sahar Sedighzadeh, Rana Saleh   +5 more
doaj   +2 more sources

Acrodermatitis enteropathica-like eruption [PDF]

JAAD Case Reports, 2022
Farah El Hadadi, MD, Line Mezni, MD, Nadia Ismaili, MD, PhD, Laila Benzekri, MD, PhD, Karima Senouci, MD, PhD   +4 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]

PLoS 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, Koen J T Venken, Robert C De Lisle, Glen K Andrews   +3 more
doaj   +6 more sources

Acrodermatitis Enteropathica

JAMA Dermatology
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   +3 more sources

Concurrence of Acrodermatitis Enteropathica and Eczema Herpeticum in a Child with Atopic Dermatitis [PDF]

Case Reports in Dermatology, 2019
Acrodermatitis enteropathica (AcE) is a rare, autosomal recessive inherited disorder caused by mutation of the SLC39A4 gene coding for zinc transport protein (ZIP 4).
Budi Satria, WenChieh Chen, Hardyanto Soebono, Sunardi Radiono, Retno Danarti   +4 more
doaj   +2 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]

BMC 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, Chao Yang, Lei Zhu, Yu-Qi Huang, Yong-Feng Chen   +4 more
doaj   +2 more sources

Acquired acrodermatitis enteropathica from a ketogenic diet [PDF]

JAAD Case Reports, 2021
Sabah Osmani, BA, Aimee C. Smidt, MD, Casey M. Phan, MD, Douglas W. Johnson, MD   +3 more
doaj   +2 more sources

Transient neonatal zinc deficiency or acrodermatitis enteropathica? [PDF]

Anais Brasileiros de Dermatologia
Luciane Francisca Fernandes Botelho, Selma Hélène, Carolina Gonçalves Contin Proença, Silvia Assumpção Soutto Mayor   +3 more
doaj   +2 more sources