Download PDF by Pooya Khan Mohammad Beigi, Emanual Maverakis: Acrodermatitis Enteropathica: A Clinician's Guide

By Pooya Khan Mohammad Beigi, Emanual Maverakis

ISBN-10: 3319178180

ISBN-13: 9783319178189

ISBN-10: 3319178199

ISBN-13: 9783319178196

This new textual content presents perception and cures for the coated affliction, together with dozens of top quality pictures, illustrations, and medical tables. subject matters coated comprise the historical past of the disorder, different types of the affliction, molecular research, epidemiology, results on physique platforms, affliction signs, and therapy. Acrodermatitis Enteropathica is an extraordinary sickness of zinc metabolism that happens in a single of 2 types: inborn and bought. If untreated, the illness is deadly and affected participants might die inside of quite a few years, yet considering there isn't any remedy for the , it really is severe that physicians are conscious of the symptoms concerning AE and the fitting remedies on hand for sufferers. A complete consultant to Acrodermatitis Enteropathica is the one e-book of its variety to provide perception into this infrequent sickness. Written through and for dermatologists, pediatric experts, and ObGYN’s, this publication comprises one of many greatest scientific examine stories performed on Acrodermatitis Enteropathica over the past decade.​

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Extra resources for Acrodermatitis Enteropathica: A Clinician's Guide

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With regards to dermatological disorders, skin eruptions and manifestations are often clear symptoms of AE: erythematous, dry, and rough pseudo psoriasis lesions are a few examples of these skin eruptions [1]. These skin manifestations are often found near the mouth, nose, eyes, ears, and perineum and termed periorificial. Pustular and vesicular lesions are the dominant forms of the dermatological symptoms of AE. Perleche is also common and can be an early sign of the disorder. Furthermore, diarrhea, abdominal pain, and foul-smelling stools are usually the first gastrointestinal symptoms of AE.

A novel zinc-regulated human zinc transporter, hZTL1, is localized to the enterocyte apical membrane. J Biol Chem. 2002;277(25):22789–97. 43. Wang K, et al. 3. Am J Hum Genet. 2001;68(4):1055–60. 44. Küry S, et al. Mutation spectrum of human SLC39A4 in a panel of patients with acrodermatitis enteropathica. Hum Mutat. 2003;22(4):337–8. 45. Grotz N, et al. Identification of a family of zinc transporter genes from Arabidopsis that respond to zinc deficiency. Proc Natl Acad Sci. 1998;95(12):7220–4.

The other form is an inheritable disease caused by a mutation in the SLC39A4 gene, which codes for the hZip4 Zn transporter protein, and it is inherited in an autosomal recessive pattern. One or more of its symptoms are often observed in the later stages of the disorder [1]. 2 Nomenclature of Zinc Deficiencies AE was identified for the first time by Brandt in 1936 [2]. In 1942, Danbolt and Closs categorized a group of symptoms as AE [3]. Furthermore, it was discovered that AE, which is an autosomal recessive inheritable disorder caused by a mutation in the gene coding for the hZip4 Zn transporter, which is necessary for zinc absorption in the intestine [4].

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Acrodermatitis Enteropathica: A Clinician's Guide by Pooya Khan Mohammad Beigi, Emanual Maverakis


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