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Results 1 - 10 of 11 for Kuster syndrome
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  1. Mayer-Rokitansky-Küster-Hauser syndrome 
    Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a disorder that mainly affects the female reproductive system. This condition causes the vagina and uterus ...
    https://medlineplus.gov/.../mayer-rokitansky-kuster-hauser-syndrome - Genetics
  2. Müllerian aplasia and hyperandrogenism 
    ... clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod. 2007 Jan;22( ... mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Kuster-Hauser syndrome). Fertil Steril. 2011 Jun 30;95(8):2683- ...
    https://medlineplus.gov/.../mullerian-aplasia-and-hyperandrogenism - Genetics
  3. LHX1 gene 
    ... females with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by underdevelopment or absence of ... disability, behavioral and psychiatric conditions, and Mayer-Rokitansky-Küster-Hauser syndrome in people with 17q12 deletion syndrome. More About ...
    https://medlineplus.gov/genetics/gene/lhx1 - Genetics
  4. 17q12 deletion syndrome 
    ... females with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by underdevelopment or absence of ... disability, behavioral and psychiatric conditions, and Mayer-Rokitansky-Küster-Hauser syndrome. The loss of other genes in the deleted ...
    https://medlineplus.gov/genetics/condition/17q12-deletion-syndrome - Genetics
  5. Chromosome 17 
    ... people with this chromosomal change have Mayer-Rokitansky-Küster-Hauser syndrome, which is characterized by the underdevelopment or absence ... disabilities, behavioral and psychiatric conditions, and Mayer-Rokitansky-Küster-Hauser syndrome. The loss of other genes in the deleted ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  6. WNT4 gene 
    ... clinical phenotype distinct from the classic Mayer-Rokitansky-Kuster-Hauser syndrome: a case report. Hum Reprod. 2007 Jan;22( ...
    https://medlineplus.gov/genetics/gene/wnt4 - Genetics
  7. SHOX gene 
    ... Condition MedlinePlus Genetics provides information about Mayer-Rokitansky-Küster-Hauser syndrome More About This Health Condition Turner syndrome occurs ...
    https://medlineplus.gov/genetics/gene/shox - Genetics
  8. Hystrix-like ichthyosis with deafness 
    ... on PubMed van Geel M, van Steensel MA, Kuster W, Hennies HC, Happle R, Steijlen PM, Konig A. HID and KID syndromes are associated with the same connexin 26 mutation. ...
    https://medlineplus.gov/.../hystrix-like-ichthyosis-with-deafness - Genetics
  9. KRT14 gene 
    ... alpha-induced apoptosis and causes Naegeli-Franceschetti-Jadassohn syndrome. J Invest Dermatol. 2008 Jun;128(6):1517-24. doi: 10.1038/sj.jid.5701187. Epub 2007 Nov 29. Citation on PubMed Muller FB, Kuster W, Wodecki K, Almeida H Jr, Bruckner-Tuderman ...
    https://medlineplus.gov/genetics/gene/krt14 - Genetics
  10. SNAI2 gene 
    ... Rodriguez-Garcia A, Gonzalez-Sanchez B, Korf BR, Kuster W, Moss C, Spritz RA, Sanchez-Garcia I. ...
    https://medlineplus.gov/genetics/gene/snai2 - Genetics
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