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3,050 Possible Causes for Kallmann Syndrome, Osteopenia, Partial or Complete Gonadotropin Deficiency

  • 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] Congenital isolated hypogonadotropic hypogonadism is characterized by partial or complete absence of pubertal development secondary to deficient gonadotropin-releasing hormone[ijdvl.com]

  • 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] Patients with AHH usually have a less complete form of gonadotropin deficiency and a larger testicular size than CHH patients.[academic.oup.com]

  • 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] Complete anosmia may therefore be associated with gonadotropin deficiency that is only partial; the presence of anosmia does not predict the need for gonadotropin therapy[ncbi.nlm.nih.gov]

  • 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] Congenital isolated hypogonadotropic hypogonadism is characterized by partial or complete absence of pubertal development secondary to deficient gonadotropin-releasing hormone[ijdvl.com]

  • 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] […] 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]

    Missing: Partial or Complete Gonadotropin Deficiency
  • 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] […] or complete lack of pubertal development, secondary to deficient GnRH-induced gonadotropin secretion, in the absence of anatomical abnormalities in the hypothalamic and pituitary[academic.oup.com]

  • 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] Treatment slows the course of osteopenia, muscle loss, vasomotor instability, loss of libido, depression, and occasionally erectile dysfunction.[msdmanuals.com] Kallmann syndrome) as well as normal puberty that is accompanied by an altered reproductive system later in life (i.e. ...[centerwatch.com]

    Missing: Partial or Complete Gonadotropin Deficiency
  • Osteoporosis

    These include Turner syndrome, Klinefelter syndrome, Kallmann syndrome, anorexia nervosa, andropause, hypothalamic amenorrhea or hyperprolactinemia.[en.wikipedia.org] Most fractures in postmenopausal women occur in those with osteopenia, so therapies that are effective in women with osteopenia are needed.[nejm.org] Tetrasomy 20p is a very rare chromosome abnormality, with only two single cases previously reported in the literature, both fetuses with multiple congenital anomalies, osteopenia[ncbi.nlm.nih.gov]

    Missing: Partial or Complete Gonadotropin Deficiency
  • Hypopituitarism

    syndrome Lymphocytic hypophysitis Transsphenoidal adenomectomy Congenital - Usually presents in childhood, but can present later with features such as delayed puberty; heritable[emedicine.com] […] some • adults • Walking and motor milestones: delayed • Hips: dysplasia; avascular necrosis of femoral head • Elbow: limited extensibility • Skin: thin, prematurely aged • Osteopenia[slideshare.net] Hypopituitarism is defined as either partial or complete deficiency of anterior or posterior pituitary hormone secretion.[arupconsult.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] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[omicsonline.org]

    Missing: Partial or Complete Gonadotropin Deficiency

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