سندرم rokitansky - kuster - hauser و گزارش چند مورد از بخش زنان و زایمان بیمارستان جرجانی
thesis
- وزارت علوم، تحقیقات و فناوری - دانشگاه شهید بهشتی
- author کمال الدین مجتبوی
- adviser پرویز معیلی
- Number of pages: First 15 pages
- publication year 1351
abstract
چکیده ندارد.
similar resources
Mayer-Rokitansky-Kuster-Hauser Syndrome.
Mayer-Rokitansky-Küster-Hauser Syndrome is a congenital malformation in which there is failure of the Müllerian ducts to develop resulting in absent uterus and fallopian tubes and variable malformations of the vagina. Ultrasonography reveals absence of uterus with normally visualised ovaries.
full textMayer-Rokitansky-Kuster-Hauser syndrome: a review
The congenital aplasia or severe hypoplasia of mullerian structures is infrequent. However, the features of normal female endocrine function paired with the absence of a functional uterus and vagina makes it a fascinating entity. The diagnosis and work-up in these patients has become very efficient, thanks to the use of imaging, and there are multiple successful procedures for the creation of a...
full textMayer-Rokitansky-Kuster-Hauser Syndrome: Surgical Management of Two Cases
The Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome is a rare anomaly characterized by congenital aplasia of the uterus and vagina in women showing normal development of secondary sexual characters and normal 44 XX karyotype. We report our experience in the management of two patients with congenital absence of the vagina due to the MRKH syndrome. The first case was a 24-year-old student, who pre...
full textMayer-Rokitansky-Kuster-Hauser syndrome associated with rectovestibular fistula
A female neonate with two openings in the introitus and an absent anal opening at the anal site presents a diagnostic challenge. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome associated with rectovestibular fistula, though rare, should be kept in mind as a differential diagnosis of this presentation. We present such a case in a one-year-old female child with MRKH syndrome and rectovestibular f...
full textAdenomyosis in a patient with the Rokitansky-Kuster-Hauser syndrome.
Endometriosis remains an enigma despite extensive clinical investigations and experience. Several theories have attempted to explain the puzzling and controversial pathogenesis of endometriosis. Sampson’s implantation theory is the most commonly accepted. Early endometriotic lesions have been found in the Douglas cavity, where retrograde menstruation was confirmed in 90% of women. These finding...
full textMayer-Rokitansky-Kuster-Hauser syndrome: recent clinical and genetic findings.
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by Mullerian duct aplasia in an XX individual with female phenotype presenting primary amenorrhea at adolescence. Multiple abnormalities may be associated with the MRKH syndrome. Genetic investigations focused on the genes of anti-Mullerian hormone and its receptor, as well as on Wt1, Pax2, Cftr and Hox genes, have been unproductiv...
full textMy Resources
document type: thesis
وزارت علوم، تحقیقات و فناوری - دانشگاه شهید بهشتی
Keywords
Hosted on Doprax cloud platform doprax.com
copyright © 2015-2023