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Results 1 - 9 of 9 for Premature ovarian failure 4
  1. FMR1 gene 
    ... end of the normal range are associated with premature ovarian failure. Hum Genet. 2005 Aug;117(4):376-82. doi: 10.1007/s00439-005-1326- ...
    https://medlineplus.gov/genetics/gene/fmr1 - Genetics
  2. Perrault syndrome 
    ... LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. Am J Hum Genet. 2013 Apr 4;92(4):614-20. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
  3. LARS2 gene 
    ... LARS2, encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome. Am J Hum Genet. 2013 Apr 4;92(4):614-20. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/lars2 - Genetics
  4. Fragile X-associated primary ovarian insufficiency 
    ... C, Sherman S. FMR1 and the continuum of primary ovarian insufficiency. Semin Reprod Med. 2011 Jul;29(4):299-307. doi: 10.1055/s-0031-1280915. ...
    https://medlineplus.gov/...-associated-primary-ovarian-insufficiency - Genetics
  5. Fragile X syndrome 
    ... C, Sherman S. FMR1 and the continuum of primary ovarian insufficiency. Semin Reprod Med. 2011 Jul;29(4):299-307. doi: 10.1055/s-0031-1280915. ...
    https://medlineplus.gov/genetics/condition/fragile-x-syndrome - Genetics
  6. NR5A1 gene 
    ... which are called spermatogenic failure in men and primary ovarian insufficiency in women, result in an inability to conceive children (infertility). AD4BP adrenal 4 binding protein ELP FTZ1 FTZF1 fushi tarazu factor ...
    https://medlineplus.gov/genetics/gene/nr5a1 - Genetics
  7. Nijmegen breakage syndrome 
    ... to moderate intellectual disability.Most affected woman have premature ovarian failure and do not begin menstruation by age 16 ( ... j.dnarep.2007.08.004. Epub 2007 Oct 4. Citation on PubMed Wolska-Kusnierz B, Gregorek H, ...
    https://medlineplus.gov/.../condition/nijmegen-breakage-syndrome - Genetics
  8. Galactosemia 
    ... GALE deficiency GALK deficiency GALT deficiency UDP-galactose-4-epimerase deficiency disease UTP hexose-1-phosphate uridylyltransferase ... Genetic Testing Registry: Galactosemia Genetic Testing Registry: UDPglucose-4-epimerase deficiency Galactosemia National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/galactosemia - Genetics
  9. Cytochrome P450 oxidoreductase deficiency 
    ... syndrome. Rev Endocr Metab Disord. 2007 Dec;8(4):301-7. doi: 10.1007/s11154-007-9056- ... and enzymatic characterization of P450 oxidoreductase deficiency in four patients. J Clin Endocrinol Metab. 2009 Dec;94( ...
    https://medlineplus.gov/...cytochrome-p450-oxidoreductase-deficiency - Genetics