Results 101 to 110 of about 1,143,195 (179)

A Mayer-Rokitansky-Kuster-Hauser Syndrome in a Neonate: A Case Report [PDF]

Iranian Journal of Neonatology
Background: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is defined as the congenital incomplete development of Müllerian structures in women who otherwise have the phenotype with a normal karyotype (46, XX), normal external genitalia, and functional ...
Nasrin Khalesi, Mandana Kashaki, Nastaran Khosravi, Zahra Vahedi, Mona Alinejad-Naeini   +4 more
doaj   +1 more source

Role of imaging in Mayer-Rokitansky-Kuster-Hauser syndrome

Medical Journal of Dr. D.Y. Patil University, 2015
Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is characterized by congenital absence of the uterus and upper 2/3 rd of vagina with a normal 46, XX karyotype and normally developed secondary sexual characteristics. It affects 1:4000 women.
Sanjay M Khaladkar, Rajesh Kuber, Dhaval K Thakkar, Anubhav Kamal, V M Kulkarni   +4 more
doaj   +1 more source

Retrograde menses presented as acute stump appendicitis- Mayer-Rokitansky-Küster-Hauser syndrome

Radiology Case Reports
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is an exceptionally rare condition. This article highlights its unusual presentation and the role of radiological imaging in the diagnosis and outlines an approach to management.
Mohammad Mohsin Arshad, MBBS, MD, Devendra Kumar, MBBS, Nouran Eltantawi, MBBS, Muhammad Junaid Iqbal, MBBS   +3 more
doaj   +1 more source

Customised Vaginal Stent-The Phases in Management of Vaginal Agenesis in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome. [PDF]

J Family Reprod Health, 2023
Raza FB, Raju K, Babu A, Vaidyanathan AK, Mehta BS.   +4 more
europepmc   +1 more source

Mullerian ducts anomaly of 2 divergent uterine horns with cervicovaginal hypoplasia: Is it considered unclassified or under the spectrum of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome? [PDF]

Radiol Case Rep, 2023
Jaha G, AlMutairi B.
europepmc   +1 more source

Προσδιορισμός γενετικών αιτιών στο σύνδρομο Mayer – Rokitansky – Küster – Hauser (MRKH): Μια συστηματική ανασκόπηση της βιβλιογραφίας

, 2022
Το σύνδρομο Mayer- Rokitansky- Küster - Hauser (MRKH) είναι μια συγγενής πάθηση που χαρακτηρίζει τις γυναίκες με απουσία της μήτρας και μέρους του κόλπου. Αρκετές γενετικές ανωμαλίες έχουν συσχετιστεί με την παρουσία MRKH.
Triantafyllidi Varvara-Ermioni, Τριανταφυλλίδη Βαρβάρα-Ερμιόνη   +1 more
core   +1 more source

RETRACTION: Mayer-Rokitansky-Kuster-Hauser (MRKH) Syndrome in a Child with Idiopathic Precocious Puberty. [PDF]

Ann Pediatr Endocrinol Metab, 2022
Kang B, Park SH, Kim DH, Lee BI, Kim MY, Lee JE.   +5 more
europepmc   +1 more source

Oestrogen-induced epithelial-mesenchymal transition (EMT) in endometriosis: Aetiology of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. [PDF]

Front Physiol, 2022
Lih Yuan T, Sulaiman N, Nur Azurah AG, Maarof M, Rabiatul Adawiyah Razali, Yazid MD.   +5 more
europepmc   +1 more source

A Case of Chromosome 17q12 Deletion Syndrome with Type 2 Mayer–Rokitansky–Küster–Hauser Syndrome and Maturity-Onset Diabetes of the Young Type 5

Children
Chromosome 17q12 deletion syndrome (OMIM #614527) is a rare genetic disorder associated with a heterozygous 1.4–1.5 Mb deletion at chromosome 17q12, leading to a spectrum of clinical manifestations, including kidney abnormalities, neurodevelopmental ...
Rosie Lee, Jung Eun Choi, Eunji Mun, Kyung hee Kim, Sun Ah Choi, Hae Soon Kim   +5 more
doaj   +1 more source

How does the experience of the medical encounter with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome impact women in Africa? [PDF]

Pan Afr Med J, 2022
Ngoumou RD.
europepmc   +1 more source