Klippel-Feil deformity, conductive deafness, and absent vagina

Known as: MRKH, Type II, Mayer-Rokitansky-Kuster-Hauser Syndrome, Type II, Mullerian Duct Aplasia, Unilateral Renal Agenesis, And Cervicothoracic Somite Anomalies 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1995-2017
01219952017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
We present a 33-year-old woman with an array of congenital abnormalities. She has been diagnosed with polycystic kidney disease… (More)
Is this relevant?
Review
2015
Review
2015
We report on a 22 years old lady with aplasia of uterus and most of the vagina with normal secondary sexual characteristics… (More)
Is this relevant?
2012
2012
We report on a 2-year-old boy who was referred to our clinic with recurrent urinary tract infections, neurogenic bladder… (More)
  • figure 2
Is this relevant?
2009
2009
 
Is this relevant?
2008
2008
Das Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrom ist durch das kongenitale Fehlen von Uterus und oberem Vaginalanteil… (More)
  • figure 1
  • figure 2
Is this relevant?
2007
2007
A 41-day-old female infant with VACTERL association was transferred to the pediatric intensive care unit of our hospital. She had… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2007
2007
We report a 15-year-old girl with features of the MURCS (Mullerian abnormalities, renal agenesis/ectopy and cervicothoracic… (More)
Is this relevant?
1999
1999
A third case of male with MURCS is described. The case is compared with two others previously reported and it is suggested that… (More)
Is this relevant?
Review
1996
Review
1996
The combination of MURCS association (Müllerian duct and renal agenesis, upper limb and rib anomalies) and occipital… (More)
Is this relevant?
1995
1995
A man with Klippel-Feil deformity, unilateral renal agenesis, and azoospermia is presented as a possible case of MURCS. 
Is this relevant?