MURCS association

MURCS association (a variant of Mayer-Rokitansky-Küster-Hauser syndrome) is a very rare developmental disorder[1] that primarily affects the reproductive and urinary systems involving MUllerian agenesis, Renal agenesis, Cervicothoracic Somite abnormalities.[2] It affects only females.

Genetics

Genetic heterogeneity is observed in MURCS association.[3]

Notes

  1. "MURCS association". Genetic and Rare Diseases Information Center (GARD). Retrieved 1 November 2013.
  2. 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.
  3. 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.

References

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