Results 71 to 80 of about 1,143,195 (179)
, 2008 International audienceThe Mayer-Rokitansky-K?r-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (two-third) of the vagina.
Guerrier, Daniel +4 more
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Germ Cell Tumors Ovary “Dysgerminoma” with Mayer-Rokitansky-Kuster-Hauser Syndrome
Magna Medika, 2023 Background: Ovarian Germ Cell Tumors originate from primitive germinal cells and can be either malignant or benign. MRKH syndrome is characterized by congenital hypoplasia of the uterus and upper vagina and can occur due to disrupted fusion of the ...
Rijanto Agoeng Basoeki +6 more
doaj +1 more source
Journal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.ABSTRACT Adenomyosis is a prevalent disorder of the archimetra, historically conflated with endometriosis but possessing a unique pathobiological trajectory. This review synthesises current molecular evidence to propose a unified mechanistic framework initiated by tissue injury and repair (TIAR), aberrant stem cell activation, or de novo metaplasia ...
Jiang Yang +6 more
wiley +1 more source
Association of single nucleotide polymorphisms with risk of MRKH syndrome in Chinese population.
, 2015 Association of single nucleotide polymorphisms with risk of MRKH syndrome in Chinese population.
Ya Li (194567) +6 more
core +1 more source
Ionic–Bionic Interfaces: Advancing Iontronic Strategies for Bioelectronic Sensing and Therapy
Advanced Science, Volume 13, Issue 16, 18 March 2026.Ionic–bionic interfaces for bioelectronics leverage ions as multifunctional mediators that combine mechanical compliance, ionic and electronic functionalities, and therapeutic effects. These systems offer real‐time biosignal transduction, effective wound dressing, responsive drug delivery, and seamless interaction between soft tissues and electronic ...
Yun Goo Ro +6 more
wiley +1 more source
ISOLATED MAYER-ROKITANSKY-KUSTER-HAUSER (MRKH) SYNDROME: A CASE REPORT AND REVIEW OF THE LITERATURE.
, 2018 Introduction: Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a congenital disorder of unknown etiology, characterized by mullerian agenesis and can be associated with renal, skeletal and cardiac malformation. Most cases are sporadic. Case Report: We
*Dr. Abiha Ahmad Khan, Prof. S. A. Naaz, Prof. Wajeeha Begum
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, 2021 The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is the most severe form of congenital malformation of the inner female reproductive tract. It is diagnosed as such when the uterus, the upper vagina and optionally the Fallopian tubes are absent. It
Karine Morcel, Daniel Guerrier*
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Συγγενείς ανωμαλίες μήτρας-σύνδρομο MRKH.
, 2018 ΣΥΝΔΡΟΜΟ ΜRKH KAI ΚΛΙΝΙΚΕΣ ΕΚΔΗΛΩΣΕΙΣ ΣΧΕΤΙΖΟΜΕΝΕΣ ΜΕ ΑΥΤΟ. Σύγγελος Ν, Ελευθεριάδης Μ, Πανουλής Κ, Δεληγεώρογλου Ε,Κρεατσάς Γ. Στοιχεία εμβρυολογίας γεννητικού συστήματος θήλεως.Περιγραφή των συγγενών ανωμαλιών μήτρας.To σύνδρομο MRKH ...
Σύγγελος Νικόλαος +1 more
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Understanding the Diagnostic Odyssey of Women with Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome in Denmark: A Qualitative Interview Study [PDF]
STUDY OBJECTIVE: The diagnosis of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is often a lengthy process that typically occurs during late adolescence. To support optimized and patient-centered care, this study aimed to investigate how women with MRKH
Vogel, Ida +4 more
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Chronic Obstructive Uropathy Complicating Complete Androgen Insensitivity Syndrome: A Case Report
Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Complete androgen insensitivity syndrome (CAIS) is a rare X‐linked difference of sex development (DSD) caused by pathogenic variants in the androgen receptor (AR) gene, leading to complete androgen resistance. Diagnosis is often delayed in low‐resource settings due to a low index of suspicion and lack of access to diagnostic testing.
Brook Alemayehu Tesfaye +5 more
wiley +1 more source