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537 Possible Causes for Anosmia, Kallmann Syndrome, Osteopenia

  • Hypogonadotropic Hypogonadism Type 18

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[uniprot.org] syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com] Women with hypogonadotropic hypogonadism are at a high risk of dislipidemia, urogenital disorders and osteopenia.[endocrine-abstracts.org]

  • Hypogonadotropic Hypogonadism Type 21

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[uniprot.org] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] 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

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[malacards.org] Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[thieme-connect.com] Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia ; Hypogonadotrophic hypogonadism ; Hypoplasia of the uterus ; Micropenis ; Osteopenia[mousephenotype.org]

  • Kallmann Syndrome

    Kallmann syndrome (KS) is a genetic gonadotropin-releasing hormone deficiency associated with hyposmia or anosmia and characterized by various modes of inheritance.[ncbi.nlm.nih.gov] 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]

  • Kallmann Syndrome Type 3

    Kallmann syndrome (KS) is a rare genetic disorder characterized by hypogonadotropic hypogonadism associated with anosmia or hyposmia.[radiopaedia.org] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.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]

  • Kallmann Syndrome Type 4

    Back to results Hypogonadotropic hypogonadism 4 with or without anosmia (sequence analysis of PROK2 gene) PROK2 Request Now Methodology Sanger sequencing Specimen Requirements[cgcgenetics.com] Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[omicsonline.org]

  • Hypogonadotropic Hypogonadism Type 22

    BACKGROUND: Congenital hypogonadotropic hypogonadism (CHH) is classified as Kallmann syndrome (KS) with anosmia/hyposmia or normosmic (n)CHH.[ncbi.nlm.nih.gov] Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005;25:98–9. PubMed Crossref Google Scholar 3.[degruyter.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]

  • Hypogonadotropic Hypogonadism

    Neuroendocrinology: PDF Only Abstract Kallmann's syndrome is a form of idiopathic hypogonadotropic hypogonadism (IHH) associated with hyposmia or anosmia.[journals.lww.com] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] 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]

  • Hypogonadism

    […] eunuchoidism, male hypogonadism the state of being a eunuch (either because of lacking testicles or because they failed to develop) Kallman's syndrome hypogonadism with anosmia[vocabulary.com] 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] Treatment slows the course of osteopenia, muscle loss, vasomotor instability, loss of libido, depression, and occasionally erectile dysfunction.[msdmanuals.com]

  • Hypogonadotropic Hypogonadism Type 20

    Anosmia or hyposmia is related to the absence or hypoplasia of the olfactory bulbs and tracts.[malacards.org] Prognosis - Kallmann syndrome - type 1 Treatment - Kallmann syndrome - type 1 Resources - Kallmann syndrome - type 1[checkorphan.org] 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]

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