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457 Possible Causes for Kallmann Syndrome, Micropenis, Osteopenia

  • Hypogonadotropic Hypogonadism Type 18

    Infant boys with congenital IGD often have micropenis and cryptorchidism.[ncbi.nlm.nih.gov] 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

    Cryptorchidism ; Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia ; Hypogonadotrophic hypogonadism ; Hypoplasia of the uterus ; Micropenis[mousephenotype.org] 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] These symptoms, such as micropenis in this case, can be useful in differentiating IHH and CDP.[omicsonline.org]

  • Kallmann Syndrome

    The authors report a case of a 26-year-old Filipino male who presented with eunuchoid body proportion, absence of facial and axillary hair and sparse pubic hair, micropenis[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]

  • Hypogonadotropic Hypogonadism Type 21

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] Clinical description Most cases are diagnosed at the time of puberty due to lack of sexual development, but KS may also be suspected in infancy in males with cryptorchidism, micropenis[orpha.net] 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 Type 3

    […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org] These symptoms, such as micropenis in this case, can be useful in differentiating IHH and CDP.[omicsonline.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]

  • Hypogonadism

    This is a case of 19 years male who presented with micropenis, marked gynaecomastia and weight gain.[ncbi.nlm.nih.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 2

    Corresponding symptoms are mainly noted in males and may comprise micropenis and cryptorchidism.[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] The clinical spectrum of 5a-RD is heterogeneous, ranging from the classic phenotype to males with hypospadias and even isolated micropenis.[ajandrology.com]

  • Kallmann Syndrome Type 4

    These symptoms, such as micropenis in this case, can be useful in differentiating IHH and CDP.[omicsonline.org] Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.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]

  • Hypogonadotropic Hypogonadism

    We report a male neonate with no family history of reproductive disorders who was born with micropenis and cryptorchidism.[ncbi.nlm.nih.gov] 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 20

    Infant boys with congenital IGD often have micropenis and cryptorchidism.[ncbi.nlm.nih.gov] Prognosis - Kallmann syndrome - type 1 Treatment - Kallmann syndrome - type 1 Resources - Kallmann syndrome - type 1[checkorphan.org] Clinical description Most cases are diagnosed at the time of puberty due to lack of sexual development, but KS may also be suspected in infancy in males with cryptorchidism, micropenis[orpha.net]

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