Asymptomatic uretheral intercourse associated with Mayer Rokitansky Küster Hauser syndrome type II: A case with crossed fused renal ectopia and scoliosis
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چکیده
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 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...
متن کامل[Mayer-Rokitansky-Küster-Hauser syndrome: A case report].
disorder. At clinical examination, the patient demonstrated a development of secondary sexual characteristics compatible with her chronological age. At gynecological examination a grooved urethra with elevated edges was observed. Speculum examination was not performed. Transabdominal ultrasonography did not demonstrate the presence of uterus and ovaries in their habitual site, but the study was...
متن کاملHereditary renal adysplasia, pulmonary hypoplasia and Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a case report
BACKGROUND Hereditary renal adysplasia is an autosomal dominant trait with incomplete penetrance and variable expression that is usually associated with malformative combinations (including Müllerian anomalies) affecting different mesodermal organs such as the heart, lung, and urogenital system. CASE REPORT A case showing pulmonary hypoplasia, hip dysplasia, hereditary renal adysplasia, and M...
متن کاملCoffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome: a case report
INTRODUCTION We report the case of an unusual association of Coffin-Siris syndrome with Mayer-Rokitansky-Küster-Hauser syndrome. This association has never previously been reported in the medical literature. CASE PRESENTATION A nine-year-old Indian girl was referred to our hospital for growth retardation, mental retardation, lax joints, generalized hypertrichosis, and hypoplastic fifth finger...
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ژورنال
عنوان ژورنال: African Journal of Urology
سال: 2017
ISSN: 1110-5704
DOI: 10.1016/j.afju.2016.03.005