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126 Possible Causes for Delayed Female Puberty, Kallmann Syndrome, Osteopenia

  • Kallmann Syndrome

    Systemic: Delayed female puberty and secondary sexual characteristics are the chief complaints in Kallmann syndrome.[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

    HH is not to be confounded with delayed male puberty or delayed female puberty due to physiological variance, nutrient deficiencies, overweight/obesity or systemic diseases[symptoma.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]

  • Hypogonadotropic Hypogonadism Type 21

    See also [ edit ] Hypogonadism Hypogonadotropic hypogonadism Hypergonadotropic hypergonadism Delayed puberty and infertility Hypothalamus, pituitary gland, and HPG axis Gonads[en.wikipedia.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 18

    Delayed puberty: analysis of a large case series from an academic center. J Clin Endocrinol Metab 87:1613-1620, 2002. 4. Grinspon RP, Rey RA.[siicsalud.com] 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 8

    E29.8 Other testicular dysfunction E29.9 Testicular dysfunction, unspecified E30 Disorders of puberty, not elsewhere classified E30.0 Delayed puberty Constitutional delay[apps.who.int] 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]

  • Anterior Pituitary Hypofunction

    puberty - adult females have Secondary Amenorrhea; produces osteoporosis, hot flashes (lack of Estrogen), decreased libido - males have impotence, due to decreased libido[quizlet.com] 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]

  • Hypogonadism

    Health problems that may result from HH include: Delayed puberty Early menopause (in females) Infertility Low bone density and fractures later in life Low self-esteem due[medlineplus.gov] 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 Type 3

    See also [ edit ] Hypogonadism Hypogonadotropic hypogonadism Hypergonadotropic hypergonadism Delayed puberty and infertility Hypothalamus, pituitary gland, and HPG axis Gonads[en.wikipedia.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]

  • Panhypopituitarism

    Left untreated, growth hormone deficiency may lead to short stature and delayed puberty.[mountsinai.org] Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of gonadotropin Isolated deficiency of growth hormone Isolated deficiency of pituitary hormone Kallmann's[icd10data.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]

  • Hypogonadotropic Hypogonadism Type 22

    See also [ edit ] Hypogonadism Hypogonadotropic hypogonadism Hypergonadotropic hypergonadism Delayed puberty and infertility Hypothalamus , pituitary gland , and HPG axis[en.wikipedia.org] 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]

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