Results 11 to 20 of about 2,564 (144)

Clinical analysis of 20 cases of childhood acrodermatitis enteropathica

open access: yesPifu-xingbing zhenliaoxue zazhi
Objective To investigate the clinical features of acrodermatitis enteropathica (AE). Methods A retrospective analysis was conducted on the clinical data of 20 children diagnosed with acrodermatitis enteropathica in the outpatient clinic at the ...
Jibing LI   +6 more
doaj   +2 more sources

Hereditary Acrodermatitis Enteropathica In Two Siblings

open access: yesIndian Journal of Dermatology, 2003
Acrodermatitis enteropathica is a rare hereditary disorder of zinc metabolism characterized by dermatitis involving the acral and periorificial skin, diarrhea and growth retardation. Two siblings with classical features of acrodermatitis enteropathic and
Masood Quzi, Majid Imran
doaj   +1 more source

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

open access: yesBMC 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   +5 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

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

open access: yesCase 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   +4 more
doaj   +2 more sources

Clinical variants of acrodermatitis enteropathica and its co-relation with genetics

open access: yesIndian Journal of Paediatric Dermatology, 2016
Acrodermatitis enteropathica (AE) is a rare disorder of zinc deficiency, which manifests as acral and periorificial dermatitis, alopecia, intractable diarrhea, and failure to thrive.
Sarabjit Kaur   +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]

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   +2 more sources

Zinc Deficiency with Acrodermatitis Enteropathica-like Eruption After Pancreaticoduodenectomy

open access: yesJournal of the Formosan Medical Association, 2007
Pancreaticoduodenectomy (PD) is the standard operation for periampullary lesions. Most reports have focused on the clinical outcome, complications and tumor recurrence after PD.
Hsin-Hsien Yu   +2 more
doaj   +2 more sources

Acquired acrodermatitis enteropathica from a ketogenic diet [PDF]

open access: yesJAAD Case Reports, 2021
Sabah Osmani, BA   +3 more
doaj   +2 more sources

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