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465 Possible Causes for Kallmann Syndrome, Male Hypogonadism, Osteopenia

  • 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] Women with hypogonadotropic hypogonadism are at a high risk of dislipidemia, urogenital disorders and osteopenia.[endocrine-abstracts.org]

  • Hypogonadotropic Hypogonadism Type 21

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Fast facts on male hypogonadism Here are some key points about male hypogonadism. More detail is in the main article.[medicalnewstoday.com] Osteopenia MedGen UID: 148180 • Concept ID: C0747078 • Disease or Syndrome Osteopenia is a term to define bone density that is not normal but also not as low as osteoporosis[ncbi.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism Type 8

    Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[thieme-connect.com] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[dnatesting.uchicago.edu] Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia ; Hypogonadotrophic hypogonadism ; Hypoplasia of the uterus ; Micropenis ; Osteopenia[mousephenotype.org]

  • 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] Osteopenia and reduced vitamin D levels of 21 nmol/L were identified. He was found to harbor a heterozygous factor-V-Leiden mutation.[ncbi.nlm.nih.gov]

  • Hypogonadism

    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] MALE HYPOGONADISM 2.[slideshare.net] Treatment slows the course of osteopenia, muscle loss, vasomotor instability, loss of libido, depression, and occasionally erectile dysfunction.[msdmanuals.com]

  • Kallmann Syndrome Type 3

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[quizlet.com] Osteopenia was equally severe in men with immature and mature bone ages, suggesting that abnormal bone development plays an important role in the osteopenia of men with idiopathic[annals.org]

  • 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] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[omicsonline.org]

  • Primary Male Hypogonadism

    Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[froedtert.com] Aim: The creation of new experimental model of primary male hypogonadism.[ingentaconnect.com] Finkelstein JS, Neer RM, Biller BMK, Crawford JD, Klibanski A: Osteopenia in men with a history of delayed puberty. N Engl J Med 1992;326:600–604.[karger.com]

  • 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] Osteopenia was equally severe in men with immature and mature bone ages, suggesting that abnormal bone development plays an important role in the osteopenia of men with idiopathic[annals.org]

  • Luteinizing Hormone Deficiency

    This disorder featuring lack of sense of smell is called anosmia or Kallmann syndrome.[healthhype.com] LH mediated high intra-testicular testosterone is essential for postnatal male sexual maturation and spermatogenesis.[endocrine-abstracts.org] The estrogen depletion that comes with menopause results in an increased risk for low bone mineral density, osteopenia and osteoporosis.[menopause.northwestern.edu]

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