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  4. Навчально-методичні видання. Кафедра медичної генетики
Please use this identifier to cite or link to this item: http://repo.knmu.edu.ua/handle/123456789/25155
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dc.contributor.authorGrechanina, Elena-
dc.contributor.authorGrechanina, Juliya-
dc.contributor.authorMolodan, Ludmila-
dc.contributor.authorZdybskaya, Olena-
dc.contributor.authorBugaeva, Olena-
dc.contributor.authorEfremova, Olesya-
dc.contributor.authorOliinyk, Daria-
dc.date.accessioned2019-12-02T07:28:54Z-
dc.date.available2019-12-02T07:28:54Z-
dc.date.issued2019-
dc.identifier.citationPorphyria : Guidelines in the discipline "Medical genetics" for the training of interns, 5th year students and cadet doctors of postgraduate education cycles / comp.: Ye. Ya. Grechanina, Yu. B. Grechanina, S. V. Beletskaya, L. V. Molodan, Ye. P. Zdybskaya, E. V. Buhaiova, O. A. Efremova, D. V. Oliinyk. – Kharkov : KhNMU, 2019. – 22 с.ru_RU
dc.identifier.urihttps://repo.knmu.edu.ua/handle/123456789/25155-
dc.descriptionЗатверджено вченою радою ХНМУ. Протокол № 8 від 19.09.2019.ru_RU
dc.description.abstractPorphyria is a group of hereditary diseases that are based on a violation of heme biosynthesis, which leads to excessive accumulation of porphyrins and their precursors in the body, namely, porphobilinogen (PBG) and δ-amino-levulinic acid (ALA). Excess of these substances has a toxic effect on the body and causes characteristic clinical symptoms. The reason for this violation is the 8 utation of the gene responsible for the activity of one of the enzymes involved in multistage heme synthesis.ru_RU
dc.language.isoenru_RU
dc.subjectPorphyriaru_RU
dc.subjectImpaired porphyrin and bilirubin metabolism (E80)ru_RU
dc.subjectМР2019ru_RU
dc.titlePorphyria : Guidelines for the training of interns, 5th year studentsru_RU
dc.title.alternativeПорфірія : методичні вказівки для підготовки лікарів-інтернів, студентів 5-го курсуru_RU
dc.typeGuidelinesru_RU
Appears in Collections:Навчально-методичні видання. Кафедра медичної генетики

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