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32 Possible Causes for Kallmann Syndrome, Male Hypogonadism, Mutation in the PROK2 Gene

  • Kallmann Syndrome

    Kallmann syndrome is the result of a genetic defect.[symptoma.com] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org] We present a case of a 22-year old man with absent puberty due to KS, in whom genetic testing revealed heterozygosity for a mutation in the PROK2 gene.[ncbi.nlm.nih.gov]

  • Kallmann Syndrome Type 4

    Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Kallmann Syndrome Type 3

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[quizlet.com]

  • Hypogonadotropic Hypogonadism Type 8

    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] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[dnatesting.uchicago.edu] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Hypogonadotropic Hypogonadism Type 18

    syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com] (For presentation in adulthood, see Male Hypogonadism : Symptoms and Signs .)[merckmanuals.com] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Luteinizing Hormone Deficiency

    This disorder featuring lack of sense of smell is called anosmia or Kallmann syndrome.[healthhype.com] Several genes have been linked to KS pathogenesis, including FGFR1, FGF8, PROK2, PROKR2, CHD7 and KAL1. 1, 2, 3, 4, 5, 6 Increasing evidence shows that overlapping genotypes[nature.com] LH mediated high intra-testicular testosterone is essential for postnatal male sexual maturation and spermatogenesis.[endocrine-abstracts.org]

  • Hypogonadotropic Hypogonadism Type 22

    Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005;25:98–9. PubMed Crossref Google Scholar 3.[degruyter.com] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org] Mutation screening KS patients were screened for mutations in genes KAL1, FGFR1, FGF8, PROK2, PROKR2, CHD7, and WDR11 as described [24].[journals.plos.org]

  • Hypogonadotropic Hypogonadism Type 21

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype-phenotype correlations. Front Horm Res 2010;39:121–32.[degruyter.com] Fast facts on male hypogonadism Here are some key points about male hypogonadism. More detail is in the main article.[medicalnewstoday.com]

  • Hypogonadotropic Hypogonadism

    Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Abstract Male hypogonadism is defined as the deficiency of testosterone or sperm production synthesized by testicles or the deficiency of both.[ncbi.nlm.nih.gov] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Ichthyosis and Male Hypogonadism

    Kallmann syndrome.[emedicine.medscape.com] Kallmann syndrome caused by mutations in the PROK2 and PROKR2 genes: pathophysiology and genotype–phenotype correlations. Front. Horm. Res. 39, 121–132 (2010). 8.[nature.com] Homepage Rare diseases Search Search for a rare disease Ichthyosis-male hypogonadism syndrome ORPHA:431 Synonym(s): - Prevalence: - Inheritance: - Age of onset: - ICD-10:[orpha.net]

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