Rare cause of woman amenorrhoea: Mayer-Rokitansky-Küster-Hauser syndrome
نویسندگان
چکیده
Uterine malformations are developmental abnormalities of the Müllerian ducts. It is a heterogeneous group pathology and anatomy whose diagnosis must be accurate. Imaging plays an essential role in with 2D/3D ultrasound magnetic resonance imaging (MRI) gold standard accurate diagnosis. We reported two cases uterine about Mayer-Rokitansky-Küster-Hauser syndrome 20-year-old patient 22-year-old patient. These anomalies associated renal malformations. The was made by chance, MRI which performed these patients. management includes psychological support component. There non-surgical treatment, but also, depending on malformation, surgical treatment. complications dominated recurrent miscarriages infertility.
منابع مشابه
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. It affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently associated with renal, vertebral, and, to a lesser ext...
متن کاملClinical and genetic aspects of Mayer–Rokitansky–Küster–Hauser syndrome
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome [MIM 277000] is characterised by the absence of a uterus and vagina in otherwise phenotypically normal women with karyotype 46,XX. Clinically, the MRKH can be subdivided into two subtypes: an isolated or type I form can be delineated from a type II form, which is characterised by extragenital malformations. The so-called Müllerian hypoplasia, r...
متن کاملGenetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome, also referred to as Müllerian agenesis, is the second most common cause of primary amenorrhea. It is characterized by congenital absence of the uterus, cervix, and the upper part of the vagina in otherwise phenotypically normal 46,XX females. MRKH syndrome has an incidence of about 1 in 4,500-5,000 newborn females and it is generally divided into ...
متن کاملMayer-Rokitansky-Küster-Hauser syndrome: fertility counseling and treatment.
To date, no literature has focused on the counseling of patients with Mayer-Rokitansky-Küster-Hauser syndrome as relates to their unique fertility challenges. This article is presented as a guide to practitioners in the counseling of patients with varying Mayer-Rokitansky-Küster-Hauser phenotypes regarding individual reproductive potential.
متن کاملEndometriosis in a Patient with Mayer-Rokitansky-Küster-Hauser Syndrome
Objective. To report a case of Mayer-Rokitansky-Küster-Hauser syndrome (MRKH) in which there were two nonfunctional rudimentary uteruses with the presence of ovarian endometrioma, corroborating that there are valid alternative theories to the existence of endometriosis, rather than Sampson's theory alone, such as the coelomic metaplasia theory. Design. A case report. Setting. A tertiary referra...
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ژورنال
عنوان ژورنال: International Journal of Case Reports and Images
سال: 2022
ISSN: ['0976-3198']
DOI: https://doi.org/10.5348/101294z01rt2022cs