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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/8699
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dc.contributor.authorBivol, Grigore
dc.contributor.authorVetrilă, R.
dc.contributor.authorArteni, Ion
dc.date.accessioned2020-04-24T14:26:02Z
dc.date.available2020-04-24T14:26:02Z
dc.date.issued2012
dc.identifier.citationBIVOL, Gr., VETRILĂ, R., ARTENI, I. Sindromul Turner (disgenezia gonadală) – patologie rară in practica medicului de familie. In: Curierul Medical. 2012, nr. 3(327), pp. 43-48. ISSN 1875-0666.en_US
dc.identifier.issn1875-0666
dc.identifier.urihttp://moldmedjournal.md/wp-content/uploads/2016/09/18.pdf
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/8699
dc.descriptionDepartment of Family Medicine, Nicolae Testemitanu State Medical and Pharmaceutical University, Congresul III al Medicilor de Familie din Republica Moldova, 17–18 mai, 2012, Chişinău, Republica Moldova, Conferinţa Naţională „Maladii bronhoobstructive la copii”, consacrată profesorului universitar, doctor habilitat Victor Gheţeul, 27 aprilie, Chişinău, Republica Moldovaen_US
dc.description.abstractOne of rare genetic diseases is Turner syndrome. We describe a patient of 44 years old with Turner syndrome, iron deficiency anemia and cardiovascular abnormalities including intestinal vascular disorders. The echocardiography confirmed the pathological changes of heart, except associated infective endocarditis on altered aortic valves. The intestinal vascular changes were confirmed by laparotomy with macro- microscopic examination of the segment of the small bowel that had been resected. Patients with these lesions require echocardiography and endoscopic tests in dynamic for the purpose of early detection of the pathology complications.en_US
dc.description.abstractСиндром Тернера относится к редким генетическим заболеваниям. Нами описывается больная 44 лет с синдромом Тернера, с железодефицитной анемией и сердечно-сосудистыми аномалиями, в том числе сосудов кишечника. Патологические изменения сердца, за исключением присоединившегося инфекционного эндокардита на измененных аортальных клапанах, подтверждены эхокардиографически. Сосудистые аномалии кишечника диагностированы при лапаротомии с макро- и микроскопическим исследованием удаленного сегмента тонкой кишки. Для более раннего выявления возможных осложнений этого заболевания, пациентам с кардио-сосудистыми аномалиями необходим эхокардиографический и эндоскопический контроль в динамике.
dc.language.isoroen_US
dc.publisherMinisterul Sănătăţii al Republicii Moldova, Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu”en_US
dc.relation.ispartofCurierul Medical: Congresul III al Medicilor de Familie din Republica Moldova, 17–18 mai, 2012, Chişinău, Republica Moldova, Conferinţa Naţională „Maladii bronhoobstructive la copii”, consacrată profesorului universitar, doctor habilitat Victor Gheţeul, 27 aprilie, Chişinău, Republica Moldova
dc.subjectTurner syndromeen_US
dc.subjectclinical particularitiesen_US
dc.subjectcomplicationsen_US
dc.titleSindromul Turner (disgenezia gonadală) – patologie rară în practica medicului de familieen_US
dc.title.alternativeSindromul Turner (disgenezia gonadală) – patologie rară în practica medicului de familieen_US
dc.typeArticleen_US
Appears in Collections:Curierul Medical, 2012, Vol. 327, Nr. 3

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