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13 Possible Causes for Eunuchism, Kallmann Syndrome, Mutation in the KISS1 Receptor Gene

  • Hypogonadotropic Hypogonadism Type 8

    Applicable To Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth[icd10data.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]

  • Kallmann Syndrome

    […] the authors performed a detailed evaluation of olfactory function in a patient with Kallman Syndrome having the rare variant of partial gonadotropin deficiency (fertile eunuch[ncbi.nlm.nih.gov] 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

    257.2 Eunuchoidism 257.2 hypogonadotropic 257.2 Failure, failed Leydig's cell, adult 257.2 seminiferous tubule, adult 257.2 testis, primary (seminal) 257.2 Fertile eunuch[icd9data.com] gene (KISS1 receptor product)?[quizlet.com] A number of conditions can cause secondary hypogonadism, including: Kallmann syndrome.[mayoclinic.org]

  • Leydig Cell Hypoplasia due to LHB Deficiency

    The fertile eunuch syndrome or Pasqualini syndrome is a cause of hypogonadotropic hypogonadism caused by a luteinizing hormone deficiency.[en.wikipedia.org] Mutations of the GnRH1 gene have also been reported in patients with hypogonadotropic hypogonadism, although they are rare.[clinicalgate.com] syndrome Leydig cell hypoplasia Leydig cell hypoplasia due to LHB deficiency Leydig cell hypoplasia due to complete LH resistance Leydig cell hypoplasia due to partial LH[se-atlas.de]

  • Male Hypogonadism

    Manifestations include eunuchism, eunuchoidism, Frohlich's syndrome, amenorrhea, and incomplete development or maintenance of secondary sex characteristics. hypogonadism decreased[medical-dictionary.thefreedictionary.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]

  • Hypogonadism

    […] development of secondary sex characteristics and (in prepubertal males) a body with long legs and a short trunk Types: eunuchoidism, male hypogonadism the state of being a eunuch[vocabulary.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 Type 4

    Fertile Eunuch Syndrome. The first report of a man with the fertile eunuch variant of CIHH was in 1950 by McCullagh.[78stepshealth.us] […] 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 Type 18

    Applicable To Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth[icd10data.com] […] 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]

  • Kallmann Syndrome Type 3

    Wortsman J, Hughes LF (1996) Case report: olfactory function in a fertile eunuch with Kallmann syndrome. Am J Med Sci 311: 135–138. View Article Google Scholar 13.[journals.plos.org] gene (KISS1 receptor product)?[quizlet.com] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    […] hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). for male or female; do not routinely interpret hypogonadism in male as EUNUCHISM[reference.md] Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] Anosmia is a distinguishing characteristic of Kallmann syndrome from other subtypes of IHH.[omicsonline.org]

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