Murcs Association

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2021-01-18
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MURCS association (a variant of Mayer-Rokitansky-Küster-Hauser syndrome) is a very rare developmental disorder that primarily affects the reproductive and urinary systems involving MUllerian agenesis, Renal agenesis, Cervicothoracic Somite abnormalities. It affects only females.

Genetics

Genetic heterogeneity is observed in MURCS association.

Diagnosis

Treatment

Notes

  1. ^ RESERVED, INSERM US14 -- ALL RIGHTS. of diseases=Mayer-Rokitansky-Kuster-Hauser-syndrome-type-2&title=Mayer-Rokitansky-Kuster-Hauser-syndrome-type-2&search=Disease_Search_Simple "Orphanet: Mayer Rokitansky Kuster Hauser syndrome type 2" Check |url= value (help). www.orpha.net. Retrieved 1 August 2017.28s%29%2Fgroup+of+diseases%3DMayer-Rokitansky-Kuster-Hauser-syndrome-type-2%26title%3DMayer-Rokitansky-Kuster-Hauser-syndrome-type-2%26search%3DDisease_Search_Simple&rfr_id=info%3Asid%2Fen.wikipedia.org%3AMURCS+association" class="Z3988">
  2. ^ "MURCS association". Genetic and Rare Diseases Information Center (GARD). Retrieved 1 November 2013.
  3. ^ Mahajan, P; Kher, A; Khungar, A; Bhat, M; Sanklecha, M; Bharucha, BA (Jul–Sep 1992). "MURCS association--a review of 7 cases". Journal of Postgraduate Medicine. 38 (3): 109–11. PMID 1303407.
  4. ^ Hofstetter, G; Concin, N; Marth, C; Rinne, T; Erdel, M; Janecke, A (2008). "Genetic analyses in a variant of Mayer-Rokitansky-Kuster-Hauser syndrome (MURCS association)". Wiener klinische Wochenschrift. 120 (13–14): 435–9. doi:10.1007/s00508-008-0995-4. PMID 18726671. S2CID 9454103.