Results 1 to 10 of about 2,669 (162)

Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant [PDF]

open access: yesPediatric Reports, 2021
We present a case of a transient acquired zinc deficiency in a breast-fed, 4-month-old-male prematurely born infant, with acrodermatitis enteropathica-like symptoms such as crusted, eroded, erythemato-squamous eruption in periorificial and acral patterns.
Giovanna D’Amico   +7 more
doaj   +2 more sources

Acrodermatitis Enteropathica: A Case Report [PDF]

open access: yesOman Medical Journal, 2020
Acrodermatitis enteropathica is a rare autosomal recessive disease caused by a genetic mutation leading to zinc deficiency. Clinical manifestation includes skin lesions, diarrhea, and alopecia.
Asma Al Naamani, Tuqa Al Lawati
doaj   +2 more sources

Acute onset of blisters in an infant with acrodermatitis enteropathica: A case report [PDF]

open access: yesSAGE Open Medical Case Reports, 2021
We represent a pediatric case of the congenital disorder caused by zinc malabsorption, acrodermatitis enteropathica, presenting with acute onsetof blisters. Although blisters can be seen in this condition, it is not always a key feature and can therefore
Kristyna Cleminson   +3 more
doaj   +2 more sources

Zinc Supplementation for Acrodermatitis Enteropathica Overlapped with Psoriasiform Lesions [PDF]

open access: yesPsoriasis: Targets and Therapy
Liangzhe Wang,* Shuaijun Zou,* Yuanjie Zhu Department of Dermatology, Naval Medical Centre, Naval Medical University, Shanghai, 200052, People’s Republic of China*These authors contributed equally to this workCorrespondence: Yuanjie Zhu ...
Wang L, Zou S, Zhu Y
doaj   +2 more sources

Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation [PDF]

open access: yesFrontiers in Pediatrics, 2022
The clinical data and gene sequencing results in a child with acrodermatitis enteropathica were retrospectively reported, and the related literature was reviewed. A girl aged 9 years and 4 months presented with a repeated skin rash, mainly distributed in
Wenjing Hua   +4 more
doaj   +2 more sources

Case of olmsted syndrome with essential thrombocytosis misdiagnosed as acrodermatitis enteropathica

open access: yesIndian Journal of Dermatology, 2021
Olmsted syndrome is a rare genodermatosis. Palmoplantar keratoderma and periorificial keratodermic plaques are the most important clinical findings.
Filiz Topaloglu Demir   +5 more
doaj   +2 more sources

Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes [PDF]

open access: yesCase Reports in Dermatological Medicine, 2021
Acrodermatitis enteropathica (AE) is a rare disorder arising from inherited or acquired zinc deficiency. It is mainly characterized by acral dermatitis, periorificial dermatitis, alopecia, and gastrointestinal symptoms in the form of diarrhea.
Owen Ngalamika   +3 more
doaj   +2 more sources

Acrodermatitis Enteropathica: A Case Report. [PDF]

open access: yesMedicine (Baltimore), 2016
Acrodermatitis enteropathica is a rare genetic autosomal recessive disorder, characterized by periorificial dermatitis, alopecia, and diarrhea. It is caused by mutations in the gene that encodes a membrane protein that binds zinc. We report a 14-month-old boy, admitted for erythematous, scaly and pustular lesions, initially located in the inguinal and ...
Nistor N   +6 more
europepmc   +3 more sources

A case of acquired acrodermatitis enteropathica in a 91-year-old man [PDF]

open access: yesSAGE Open Medical Case Reports
This report is a care experience of acrodermatitis enteropathica caused by inadequate zinc intake. The male patient is 91 years old, he had been fasting caused by recurrent acute pancreatitis, and intravenous nutrition lacking zinc. The case was based on
Yi Shen   +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]

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

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