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Acrodermatitis Enteropathica [electronic resource] : A Clinician's Guide / by Pooya Khan Mohammad Beigi, Emanual Maverakis.

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dc.contributor.author Khan Mohammad Beigi, Pooya. author.
dc.contributor.author Maverakis, Emanual. author.
dc.contributor.author SpringerLink (Online service)
dc.date.accessioned 2017-12-01T03:09:43Z
dc.date.available 2017-12-01T03:09:43Z
dc.date.created 2015.
dc.date.issued 2015
dc.identifier.isbn 9783319178196
dc.identifier.uri http://dspace.conacyt.gov.py/xmlui/handle/123456789/13660
dc.description XXI, 156 p. 56 illus., 51 illus. in color.
dc.description.abstract Written by and for dermatologists, pediatric and obstetrics specialists. This book presents the groundbreaking work of Dr. Pooya Khan Mohammad Beigi M.D., whose clinical research study on Acrodermatitis Enteropathica (AE) is the largest ever conducted on this rare disorder. The only book of its kind to offer insights into AE, it not only includes dozens of high quality photographs, illustrations, and clinical tables, but also covers everything from the history of AE to categories of the disorder, molecular analysis, epidemiology, disorder signs and symptoms, diagnosis, treatment, and more. Acrodermatitis Enteropathica is a rare disorder of zinc metabolism that occurs in one of two forms: inborn and acquired. If untreated, this disease is fatal and affected individuals may die within just a few years. Therefore, it is critical that physicians are aware of the signs and symptoms related to AE and the appropriate treatments available for patients.
dc.description.tableofcontents 1. History of Acrodermatitis Enteropathica -- 2. Epidemiology and Etiology -- 2.1. Epidemiology -- 2.2. Etiology -- 2.2.1. Molecular Etiology of AE -- 2.2.2. Hypothetical Etiology 1: the Alteration of Zinc Bioavailability -- 2.2.3. Hypothetical Etiology 2: a Defective Zinc Transporter -- 2.2.4. Alternative Forms of AE-like Zinc Deficiencies -- 3. Analysis of Disorder -- 3.1. Clinical Forms of AE -- 3.2. Nomenclature of Zinc Deficiencies -- 3.3. Acquired Non-hereditary Zinc Deficiency -- 3.3.1. Zinc Deficient Maternal Breast Milk -- 3.3.2. Zinc Deficient Caused by Metabolism Disorders -- 4. Clinical Symptoms -- 5. Diagnosis -- 5.1. Laboratory Diagnosis of Zinc Deficiency -- 5.2. Histopathology -- 5.3. Biological Diagnosis of AE -- 5.4. Clinical Diagnosis -- 5.5. Molecular Diagnosis -- 5.6. Differential Diagnosis -- 6. Disease Course and Treatment -- 6.1. Treatment -- 7. The Role of Zinc in Different Body Systems -- 7.1. Biochemistry of Zinc Metabolism -- 7.2. Skin and Hair Physiology -- 7.3. Gastrointestinal System and Other Organs -- 7.4. Neurological Development, Growth, and Mental Status -- 7.5. Enzymes -- 7.6. Endocrine System -- 7.7. Metabolism of Nucleic Acids -- 7.8. Mitosis and Meiosis Cycles -- 7.9. Cell Membranes -- 7.10. Synthesis of Proteins and Collagen -- 7.11. Immune System -- 8. History of AE in Adults -- 9. Iranian Hospital Cases in Literature -- 9.1. Patient One -- 9.2. Patient Two -- 9.3. Patient Three -- 9.4. Patient Four -- 9.5. Zinc Deficiency Similarities to AE in Infants (Fifth Patient) -- 10. Clinical Research -- 10.1. Abstract -- 10.2. Synopsis of Study -- 10.3. Purpose of Study -- 10.4. The Considered Hypotheses -- 10.5. Introduction -- 10.5. Methods -- 10.6. Ethical Considerations -- 10.7. Results -- 10.8. Discussion -- 11. Evaluation of Symptoms in Razi Dermatology Hospital -- 12. Case Photos.
dc.language eng
dc.publisher Cham : Springer International Publishing : Imprint: Springer, 2015.
dc.relation.ispartofseries Springer eBooks
dc.relation.uri http://cicco.idm.oclc.org/login?url=http://dx.doi.org/10.1007/978-3-319-17819-6
dc.subject Medicine.
dc.subject Dermatology.
dc.subject Obstetrics.
dc.subject Pediatrics.
dc.subject Medicine & Public Health.
dc.subject Dermatology.
dc.subject Pediatrics.
dc.subject Obstetrics/Perinatology.
dc.subject.ddc 616.5 23
dc.subject.lcc RL1-803
dc.subject.other Medicine (Springer-11650)
dc.title Acrodermatitis Enteropathica [electronic resource] : A Clinician's Guide / by Pooya Khan Mohammad Beigi, Emanual Maverakis.
dc.type text
dc.identifier.doi 10.1007/978-3-319-17819-6
dc.identifier.bib 978-3-319-17819-6
dc.format.rdamedia computer
dc.format.rdacarrier online resource
dc.format.rda text file PDF


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