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16 Possible Causes for Erectile Dysfunction, Kallmann Syndrome, Mutation in the KISS1 Receptor Gene

  • Hypogonadotropic Hypogonadism Type 8

    dysfunction, azoospermia, Klinefelter Syndrome, varicocele, cystic fibrosis and spinal cord injury.[books.google.com] Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] Kallmann syndrome - absent puberty with no sense of smell. Me at 18 years old in my final year at school. I had not started puberty yet.[imgur.com]

  • Hypogonadism

    Hypogonadism and Erectile Dysfunction Hypogonadism can cause erectile dysfunction. It is a very important cause of impotence in males.[newyorkurologyspecialists.com] […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[ncbi.nlm.nih.gov]

  • Kallmann Syndrome

    Affected men may also report reduced libido and have problems of erectile dysfunction.[news-medical.net] Some key molecules have been discovered through the study of the genetics of CHH. 1 Inactivating mutations in genes encoding kisspeptin-1 ( KISS1 ) 40 and its receptor ( KISS1R[doi.org] Kallmann syndrome is the result of a genetic defect.[symptoma.com]

  • Primary Male Hypogonadism

    These were poor morning erection, diminished sexual thoughts, erectile dysfunction, unable to do vigorous activity, limited in walking more than 1 km, and unable to bend ([academic.oup.com] gene (KISS1 receptor product)?[quizlet.com] Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[froedtert.com]

  • Male Hypogonadism

    Does Opioid Cause Erectile Dysfunction And Infertility? Yes, long-term opioid treatment can cause erectile dysfunction (ED) and infertility.[epainassist.com] gene (KISS1 receptor product)?[quizlet.com] Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[louisville.edu]

  • Kallmann Syndrome Type 3

    They have also shown an increase in libido but not an improvement in erectile dysfunction; phosphodiesterase inhibitors may be needed.[endocrineweb.com] gene (KISS1 receptor product)?[quizlet.com] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org]

  • Kallmann Syndrome Type 4

    They have also shown an increase in libido but not an improvement in erectile dysfunction; phosphodiesterase inhibitors may be needed.[endocrineweb.com] […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism

    We report a rare case of idiopathic hypogonadotropic hypogonadism in an adult male (31-year-old), who underwent an endocrinological examination because of erectile dysfunction[ncbi.nlm.nih.gov] […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com]

  • Hypogonadotropic Hypogonadism Type 18

    The symptoms of low testosterone in men range from lack of energy, depressed mood, loss of vitality, muscle atrophy (sarcopenia), muscles aches, low libido, erectile dysfunction[tupincho.net] […] two novel missense mutations in the gene encoding the GNRH receptor ( GNRHR1 : NM_000406.2; HGNC: 4421), see Figure 2.[journals.plos.org] syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com]

  • Congenital Absence of the Penis

    Penis disorders include Erectile dysfunction - inability to get or keep an erection Priapism - a painful erection that does not go away Peyronie's disease - bending of the[icdlist.com] Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] As with a lot (but not all) men with Kallmann syndrome I have underdeveloped genitals.[kallmannsyndrome.wordpress.com]

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