{"id":20734,"date":"2026-07-31T10:33:16","date_gmt":"2026-07-31T10:33:16","guid":{"rendered":"https:\/\/woncaeurope2026.org\/sessions\/mayer-rokitansky-kuster-hauser-mrkh-syndrome-a-rare-case-report-from-xxx\/"},"modified":"2026-07-31T10:33:16","modified_gmt":"2026-07-31T10:33:16","slug":"mayer-rokitansky-kuster-hauser-mrkh-syndrome-a-rare-case-report-from-xxx","status":"publish","type":"wsa_session","link":"https:\/\/woncaeurope2026.org\/fr\/sessions\/mayer-rokitansky-kuster-hauser-mrkh-syndrome-a-rare-case-report-from-xxx\/","title":{"rendered":"Mayer-Rokitansky-K\u00fcster-Hauser (MRKH) Syndrome: A Rare Case Report from XXX"},"content":{"rendered":"<p>MRKH syndrome, or M\u00fcllerian agenesis, is a rare congenital disorder affecting 1 in 4,500\u20135,000 females, characterized by absence or underdevelopment of the uterus and upper two-thirds of the vagina, with normal 46,XX karyotype and secondary sexual characteristics. It is a leading cause of primary amenorrhea and poses diagnostic challenges in primary care. Early recognition and referral are essential to address reproductive, sexual, and psychological health needs.A 20-year-old female presented to Family Medicine clinic with primary amenorrhea and normal secondary sexual development. Examination was unremarkable. Investigations revealed vitamin D deficiency; CBC, electrolytes, liver function, vitamin B12, TSH, and karyotype (46,XX) were normal. Pelvic ultrasound suggested absent uterus; MRI confirmed MRKH type 1 with uterovaginal aplasia, normal ovaries, and rudimentary M\u00fcllerian remnants. She was referred for gynecologic evaluation, reproductive counseling, and psychological support. Strengths included early recognition and imaging; limitation was lack of long-term follow-up.MRKH syndrome is rarely reported from XXX, especially in primary care. This case highlights the family physician\u2019s role in early identification and referral, the utility of MRI for detailed anatomical assessment, and the integration of reproductive and psychological care. Unlike many reports, this patient was asymptomatic aside from primary amenorrhea, with detailed documentation of ovarian morphology and M\u00fcllerian remnants.Primary care providers can facilitate timely diagnosis and multidisciplinary management, improving patient outcomes. Awareness and structured evaluation of adolescent females with primary amenorrhea can prevent diagnostic delays, allow early counseling, and support interventions for sexual and reproductive health.MRI remains the gold standard for anatomical assessment and management planning. Psychological support is crucial given the emotional impact of MRKH diagnosis. Multidisciplinary care, including gynecology, fertility counseling, and psychosexual therapy, is essential.MRKH syndrome should be considered in adolescent females presenting with primary amenorrhea despite normal pubertal development. Early, structured evaluation, including MRI, enables accurate diagnosis, identification of associated anomalies, and timely multidisciplinary management. Integrating gynecologic care, fertility counseling, and psychological support enhances patient well-being, empowers informed decision-making, and ensures a holistic approach to sexual and reproductive health. Raising awareness in primary care can improve detection, optimize care pathways, and guide future practice in adolescent health.<\/p>\n","protected":false},"template":"","class_list":["post-20734","wsa_session","type-wsa_session","status-publish","hentry","description-off"],"_links":{"self":[{"href":"https:\/\/woncaeurope2026.org\/fr\/wp-json\/wp\/v2\/wsa_session\/20734","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/woncaeurope2026.org\/fr\/wp-json\/wp\/v2\/wsa_session"}],"about":[{"href":"https:\/\/woncaeurope2026.org\/fr\/wp-json\/wp\/v2\/types\/wsa_session"}],"wp:attachment":[{"href":"https:\/\/woncaeurope2026.org\/fr\/wp-json\/wp\/v2\/media?parent=20734"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}