Acrodermatitis

Common Name(s)

Acrodermatitis

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Acrodermatitis" for support, advocacy or research.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Acrodermatitis" returned 76 free, full-text research articles on human participants. First 3 results:

Pustules of the fingers: acrodermatitis continua.
 

Author(s): Annie Langley, Yuka Asai

Journal: CMAJ. 2016 Oct;188(15):1105.

 

Last Updated: 30 Mar 2016

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Acrodermatitis Continua of Hallopeau with Granuloma-like Vegetation, Osteolysis and IL36RN Mutation.
 

Author(s): Yumeng Qi, Li Qiu, Song Zheng, Songbai Li, Ting Xiao

Journal: Acta Derm. Venereol.. 2017 01;97(1):122-123.

 

is missing (Short communication).

Last Updated: 27 May 2016

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Acrodermatitis Enteropathica: A Case Report.
 

Author(s): Nicolai Nistor, Lavinia Ciontu, Otilia-Elena Frasinariu, Vasile Valeriu Lupu, Ancuta Ignat, Violeta Streanga

Journal: Medicine (Baltimore). 2016 May;95(20):e3553.

 

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, ...

Last Updated: 20 May 2016

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Acrodermatitis" returned 3 free, full-text review articles on human participants. First 3 results:

Iloprost administration in acrodermatitis of Hallopeau complicated by acquired toes syndactyly: a case report and review of the literature.
 

Author(s): F Segreto, D Tosi, G F Marangi, A L Pendolino, S Santoro, P Gigliofiorito, P Persichetti

Journal: Eur Rev Med Pharmacol Sci. 2015 Aug;19(16):2945-8.

 

Acrodermatitis Continua of Hallopeau (ACH) is a variant of pustular psoriasis often very difficult to treat. Secondary syndactyly, also called "pseudosyndactyly", is rare and can be a complication of burns, dystrophic epidermolysis bullosa or trauma. If left untreated, joint complications ...

Last Updated: 15 Sep 2015

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[Acrodermatitis enteropathica: report of one case].
 

Author(s): Roberto Valdés, Michelle Mauret, Álex Castro

Journal: Rev Med Chil. 2013 Nov;141(11):1480-3.

 

Acrodermatitis enteropathica is an uncommon disease caused by hereditary or acquired zinc deficiency. It is characterized by a triad of alopecia, diarrhea and acral and periorificial dermatitis. It is treated with Zinc supplementation. We report a 31-year-old indigent and drug addict ...

Last Updated: 10 Apr 2014

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Regulation and function of Zip4, the acrodermatitis enteropathica gene.
 

Author(s): Glen K Andrews

Journal: Biochem. Soc. Trans.. 2008 Dec;36(Pt 6):1242-6.

 

The SLC39A (solute carrier 39A) [ZIP (Zrt-Irt-like protein)] family consists of 14 members which are thought to control zinc uptake into the cytoplasm. Among these, ZIP4 is known to be particularly important for zinc homoeostasis. Mutations in this gene cause acrodermatitis enteropathica, ...

Last Updated: 21 Nov 2008

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Symptoms, Diagnosis, and Treatment

There are currently no related results available in GeneReviews.

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Laboratory Characteristics in Chronic Atrophic Acrodermatitis
 

Status: Recruiting

Condition Summary: Chronic Atrophic Acrodermatitis

 

Last Updated: 11 May 2016

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Borrelia Species in Cutaneous Lyme Borreliosis
 

Status: Recruiting

Condition Summary: Lyme Borreliosis

 

Last Updated: 8 Jun 2016

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