Caz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipică
Închide
Conţinutul numărului revistei
Articolul precedent
Articolul urmator
304 3
Ultima descărcare din IBN:
2023-11-05 14:35
SM ISO690:2012
CHIRIŢA, Lilia, BEJAN, Sergiu, BOBU, Victor, GUŢU, Constantin, CARAION, Vladimir, GAIDĂU, Margareta, PLEŞCA, Eduard. Caz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipică. In: Arta Medica , 2011, nr. 2S(45), pp. 154-156. ISSN 1810-1852.
EXPORT metadate:
Google Scholar
Crossref
CERIF

DataCite
Dublin Core
Arta Medica
Numărul 2S(45) / 2011 / ISSN 1810-1852 /ISSNe 1810-1879

Caz clinic: sindromul Mayer-Rokitansky-Kuster-Hauser, forma atipică

Clinical case: Mayer-Rokitansky-Kuster-Hauser syndrome, atypic form


Pag. 154-156

Chiriţa Lilia1, Bejan Sergiu2, Bobu Victor1, Guţu Constantin2, Caraion Vladimir1, Gaidău Margareta1, Pleşca Eduard2
 
1 Spitalul Clinic Municipal „Sfânta Treime”,
2 Universitatea de Stat de Medicină şi Farmacie „Nicolae Testemiţanu“
 
 
Disponibil în IBN: 28 martie 2022


Rezumat

The Mayer-Rokitansky-kuster-Hauser (MRkH) syndrome is a rare anomaly in the prenatal development of the female genital tract. In this paper we report a clinical case of this syndrome observed in its atypical form with affected urogenital system, as well as uterine and renal agenesia. This case is interesting, as the patient did not receive any specific treatment associated with the syndrome until the age of 29. We provide a detailed description of the clinical case, its specifics and anamnesis. A literature review on the prenatal development of the female genital tract, urogenital system and the renal agenesia is also given.