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31 Possible Causes for Kallmann Syndrome, Mutation in the PROK2 Gene, 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] Women with hypogonadotropic hypogonadism are at a high risk of dislipidemia, urogenital disorders and osteopenia.[endocrine-abstracts.org] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Hypogonadotropic Hypogonadism Type 8

    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] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • 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] 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]

  • Hypogonadotropic Hypogonadism Type 21

    […] 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] 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]

  • Kallmann Syndrome Type 3

    […] 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] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Kallmann Syndrome Type 4

    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] […] and psychological disturbances. [5], [6], [7], [8] In addition to being infertile, women with HH suffer from conditions associated with a low estrogenic milieu, including osteopenia[fertilityscienceresearch.org]

  • Kallmann Syndrome Type 2

    The respective patients are diagnosed with Kallmann syndrome type 2.[symptoma.com] Bone density scan ( DXA ) to check for osteoporosis or osteopenia. [3] [2] Treatment [ edit ] Testosterone gel sachets, Testosterone undecanoate injection (Nebido), Human[en.wikipedia.org] Some individuals with Kallmann syndrome have mutations in the PROK2 or PROKR2 genes.[my46.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] 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] Women with hypogonadotropic hypogonadism are at a high risk of dislipidemia, urogenital disorders and osteopenia.[endocrine-abstracts.org]

  • Hypogonadotropic Hypogonadism Type 19 

    […] 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] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

  • Hypogonadotropic Hypogonadism

    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] Homozygous loss-of function mutation in the PROK2 gene cause IHH and Kallmann syndrome [ 8 ].[omicsonline.org]

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