MURCS連合
WordNet
- the act of consorting with or joining with others; "you cannot be convicted of criminal guilt by association"
- (chemistry) any process of combination (especially in solution) that depends on relatively weak chemical bonding
- a relation resulting from interaction or dependence; "flints were found in association with the prehistoric remains of the bear"; "the host is not always injured by association with a parasite"
- the state of being connected together as in memory or imagination; "his association of his father with being beaten was too strong to break"
- the process of bringing ideas or events together in memory or imagination; "conditioning is a form of learning by association" (同)connection, connexion
- (ecology) a group of organisms (plants and animals) that live together in a certain geographical region and constitute a community with a few dominant species
- a formal organization of people or groups of people; "he joined the Modern Language Association"
PrepTutorEJDIC
- 〈U〉(…との)『交際』,付き合い《+『with』+『名』》 / 〈U〉(…との)『連合』,『共同』,関連《+『with』+『名』》 / 〈C〉組合,協会,会社 / 〈U〉連想;〈C〉《しばしば複数形で》連想されるもの
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2014/12/10 22:47:27」(JST)
[Wiki en表示]
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
- ^ "MURCS association". Genetic and Rare Diseases Information Center (GARD). Retrieved 1 November 2013.
- ^ 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.
- ^ 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
- "MURCS Association". National Organization for Rare Disorders, Inc.
- Duncan, PA; Shapiro, LR; Stangel, JJ; Klein, RM; Addonizio, JC (September 1979). "The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia.". The Journal of pediatrics 95 (3): 399–402. doi:10.1016/s0022-3476(79)80514-4. PMID 469663.
- Greene, RA; Bloch, MJ; Huff, DS; Iozzo, RV (January 1986). "MURCS association with additional congenital anomalies.". Human pathology 17 (1): 88–91. PMID 3510965.
UpToDate Contents
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English Journal
- Management of vaginal agenesis.
- Edmonds DK.SourceQueen Charlotte's and Chelsea Hospital, London, UK.
- Current opinion in obstetrics & gynecology.Curr Opin Obstet Gynecol.2013 Oct;25(5):382-7. doi: 10.1097/GCO.0b013e328363d67f.
- PURPOSE OF REVIEW: Mayer-Rokitansky-Küster-Hauser syndrome is undergoing new research outcomes involving genetics and management.RECENT FINDINGS: Recent literature supports a polygenic multifactorial genetic basis for the syndrome. Management is now predominantly by vaginal dilators and nonsurgical
- PMID 24018875
- Glioblastoma arising in a patient with Mayer-Rokitansky-Küster-Hauser syndrome.
- Gonzalez EM, Prayson RA.SourceCleveland Clinic Lerner College of Medicine of Case Western Reserve University, Cleveland, OH, USA.
- Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia.J Clin Neurosci.2013 Oct;20(10):1464-5. doi: 10.1016/j.jocn.2013.06.002. Epub 2013 Sep 7.
- Mayer-Rokitansky-Küster-Hauser syndrome is a rare developmental disorder marked by the congenital absence of the uterus and vagina. The syndrome has been associated with tumors of the female reproductive system, but rarely in other organ systems and to our knowledge, never in the brain. We report a
- PMID 24018257
- Mayer-rokitansky-küster-hauser syndrome accompanied by renal cell carcinoma: a case report.
- Mermerkaya M, Burgu B, Hamidi N, Yüksel S, Ozçakar ZB, Sertçelik A, Yalçinkaya F, Soygür T.SourceDepartments of *Urology †Pathology ‡Pediatric Nephrology, University of Ankara, School of Medicine, Ankara, Turkey.
- Journal of pediatric hematology/oncology.J Pediatr Hematol Oncol.2013 Oct;35(7):e309-10. doi: 10.1097/MPH.0b013e3182707321.
- Mayer-Rokitansky-Küster-Hauser anomaly originates from agenesis of the Müllerian duct including agenesis of the uterus and the vagina because of abnormal development of the uterine ducts. This syndrome may be accompanied by the upper urinary tract anomalies such as unilateral renal agenesis, ectop
- PMID 23042009
Japanese Journal
- A Female Infant Who Had both Complete VACTERL Association and MURCS Association : Report of a Case
- KOMURA MAKOTO,KANAMORI YUTAKA,SUGIYAMA MASAHIKO,TOMONAGA TETSUYA,SUZUKI KAN,HASHIZUME KOUHEI,GOISHI KEIGO
- Surgery today : the Japanese journal of surgery 37(10), 878-880, 2007-10-01
- NAID 10019946633
- Right esophageal lung in a preterm child with VACTERL association and Mayer-Rokitansky-Kuster-Hauser syndrome
- LINKE F.,KRAEMER W.,ANSORGE M.,BRZEZINSKA R.,BERGER S.
- Pediatric surgery international 21(4), 285-288, 2005-04-01
- NAID 10019040867
- MURCS association : case report and review
Related Links
- Most individuals with MURCS association are female, although males can also have this condition. Females with MURCS association can have an absent or abnormally shaped uterus. In rare cases, the vagina is also affected. Both males and ...
- The MURCS association: Müllerian duct aplasia, renal aplasia, and cervicothoracic somite dysplasia. Duncan PA, Shapiro LR, Stangel JJ, Klein RM, Addonizio JC. Two patients and 28 others in the literature were ascertained because of ...
★リンクテーブル★
[★]
- 英
- MURCS association
- 関
- MURCS症候群
[★]
- (共通の目的のための)協会、組合、団体、会社
- (正式)(～との)連合、合同、提携(partnership)。交際(friendship)(with)
- 関係、つながり、結びつき
- 連合、連想(されるもの)。(数学)結合。(化学)会合、対合。(言語)(意味の)連想
- (生態)群集、群叢