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69 Possible Causes for Follicle-stimulating Hormone Decreased, Kallmann Syndrome, Osteopenia

  • Kallmann Syndrome

    Kallmann syndrome is the result of a genetic defect.[symptoma.com] 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] Magnetic resonance imaging showed the absence of the olfactory bulbs, and a bone density (DEXA) scan showed osteopenia.[themighty.com]

  • Hypogonadotropic Hypogonadism

    Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] However, their decrease can be reversed by follicle-stimulating hormone. Serum AMH and AFC should not serve as prognostic markers of fertility in this population.[ncbi.nlm.nih.gov] Bone mineral density showed osteopenia. Endogenous LH secretory pattern was abnormal with low amplitude and frequency, but responded to pulsatile GnRH administration.[ncbi.nlm.nih.gov]

  • 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] Diagnosis is by measurement of serum testosterone, luteinizing hormone, and follicle-stimulating hormone and by stimulation tests with human chorionic gonadotropin or gonadotropin-releasing[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] Diagnosis is by measurement of serum testosterone, luteinizing hormone, and follicle-stimulating hormone and by stimulation tests with human chorionic gonadotropin or gonadotropin-releasing[merckmanuals.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]

  • Anterior Pituitary Hypofunction

    syndrome (hypogonadotropic hypogonadism with anosmia) 253.4 Syndrome - see also Disease Kallmann's (hypogonadotropic hypogonadism with anosmia) 253.4 Crosswalk Information[healthprovidersdata.com] Numerous studies demonstrate that longterm use of thyroid hormone significantly increases bone loss and conditions associated with osteopenia.[metabolichealing.com] Osteopenia.[cancer.gov]

  • 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] hormone (FSH) and luteinizing hormone (LH), by the pituitary gland in the brain, and in turn decreased gonadotropin levels and a resultant lack of sex steroid production.[naturalheightgrowth.com] Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia ; Hypogonadotrophic hypogonadism ; Hypoplasia of the uterus ; Micropenis ; Osteopenia[mousephenotype.org]

  • 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] Fe iron; FSH follicle-stimulating hormone; GnRH gonadotropin-releasing hormone; LH luteinizing hormone.[msdmanuals.com] Kallmann syndrome) as well as normal puberty that is accompanied by an altered reproductive system later in life (i.e. ...[centerwatch.com]

  • Kallmann Syndrome Type 4

    Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov] HH is caused by decreased release or function of gonadotropin-releasing hormone (GnRH), which results in decreased gonadotropin production in the pituitary, including follicle[clinicaladvisor.com] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[omicsonline.org]

  • Kallmann Syndrome Type 3

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Diagnosis is by measurement of serum testosterone, luteinizing hormone, and follicle-stimulating hormone and by stimulation tests with human chorionic gonadotropin or gonadotropin-releasing[msdmanuals.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]

  • Panhypopituitarism

    Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth hormone Isolated deficiency of pituitary hormone Kallmann's[icd10data.com] Follicle-stimulating hormone (FSH) and luteinizing hormone (LH) deficiency typically presents as amenorrhea, atrophic vaginitis, infertility, hot flushes and breast atrophy[medicaljoyworks.com] […] pubertal development Delayed pubertal growth Pubertal delay [ more ] 0000823 Delayed skeletal maturation Delayed bone maturation Delayed skeletal development [ more ] 0002750 Osteopenia[rarediseases.info.nih.gov]

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