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Results 1 - 6 of 6 for "Mayer-Rokitansky-Küster-Hauser" syndrome type 2
  1. ... Hauser (MRKH) syndrome. Clin Genet. 2017 Feb;91(2):233-246. doi: ... I Mayer-Rokitansky-Kuster-Hauser syndrome. Genet Med. 2010 Oct;12(10):634-40. ...
  2. ... diabetes called maturity-onset diabetes of the young type 5 (MODY5), delayed development, intellectual disability, and behavioral or psychiatric disorders. Some females with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by underdevelopment or absence of ...
  3. ... diabetes called maturity-onset diabetes of the young type 5 (MODY5); delayed development; intellectual disability; and behavioral or psychiatric disorders. Some females with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by underdevelopment or absence of ...
  4. ... missing vagina is most often due to Mayer-Rokitansky-Kuster-Hauser ... include having 2 vaginas or a vagina that opens into the ...
  5. ... a clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod. 2007 Jan;22( ... D. WNT4 and sex development. Sex Dev. 2008;2(4-5):210-8. doi: 10.1159/000152037. ...
  6. ... intellectual disability, behavioral and psychiatric conditions, and Mayer-Rokitansky-Küster-Hauser syndrome. The loss of other genes in the deleted ...