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634 Possible Causes for Hirsutism, Kallmann Syndrome, Osteopenia

  • Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum

    PROKR2) Kallmann syndrome 3 KAL4 (offiz. PROK2) Hypogonadism, hypogonadotropic Kallmann syndrome 4 KAL5 (off.[uniklinik-freiburg.de] Most people with MONA develop low bone mineral density (osteopenia) and thinning of the bones (osteoporosis) throughout the skeleton.[ncbi.nlm.nih.gov] Additional features include coarse face, corneal opacities, patches of thickened, hyperpigmented skin, hypertrichosis and gum hypertrophy.[malacards.org]

  • 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] Modest weight loss can lower androgen levels, improve hirsutism, normalize menses, and decrease insulin resistance.[aafp.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] An abdominal CT and DEXA scan revealed undescended testes and osteopenia, respectively. He was diagnosed as IHH.[omicsonline.org]

  • 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] Modest weight loss can lower androgen levels, improve hirsutism, normalize menses, and decrease insulin resistance.[aafp.org]

  • Hypertrichotic Osteochondrodysplasia

    […] abnormalities , see Woodhouse-Sakati syndrome hypogonadotropic hypogonadism and anosmia , see Kallmann syndrome hypogonadotropic hypogonadism-anosmia syndrome , see Kallmann[herenciageneticayenfermedad.blogspot.com] Hirsutism of the lower back (B) and forearms(C) Figure 3 All images are from a woman age 40 years.[ncbi.nlm.nih.gov] Thickened calvarium, narrow thorax, wide ribs, flattened or ovoid vertebral bodies, coxa valga, osteopenia, enlarged medullary canals, and metaphyseal widening of long bones[diseaseinfosearch.org]

  • Winchester Syndrome

    Williams syndrome Autosomal recessive limb girdle muscular dystrophy type 2A Hartsfield-Bixler-Demyer syndrome Isolated trigonocephaly Kallmann syndrome Myeloid neoplasm[csbg.cnb.csic.es] […] content Torg-Winchester syndrome Joe Segen 2016-11-28T07:07:36 00:00 ORTHOPAEDICS An autosomal recessive disorder (OMIM:259600) characterised by generalised osteolysis and osteopenia[newmedicalterms.com] An autosomal recessive syndrome (OMIM:259600) characterised by generalised osteolysis and osteopenia, coarse face, corneal opacities, patches of thickened, hyperpigmented[medical-dictionary.thefreedictionary.com]

  • 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] Modest weight loss can lower androgen levels, improve hirsutism, normalize menses, and decrease insulin resistance.[aafp.org]

  • Michels-Caskey Syndrome

    Juvenile primary lateral sclerosis Juvenile retinoschisis Juvenile-onset dystonia Kabuki syndrome Kallmann syndrome Kallmann syndrome 1 Kallmann syndrome 2 Kanzaki disease[rarediseases.info.nih.gov] […] seizures, and brain atrophy Potassium aggravated myotonia Potato nose Potocki-Lupski syndrome Potocki-Shaffer syndrome Potter sequence PPM-X syndrome Prader-Willi habitus, osteopenia[rarediseases.info.nih.gov] […] syndrome Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Acromegaloid facial appearance syndrome Acromegaloid features, overgrowth, cleft palate and hernia Acromegaloid hypertrichosis[rarediseases.info.nih.gov]

  • Bagatelle-Cassidy Syndrome

    Juvenile primary lateral sclerosis Juvenile retinoschisis Juvenile-onset dystonia Kabuki syndrome Kallmann syndrome Kallmann syndrome 1 Kallmann syndrome 2 Kanzaki disease[rarediseases.info.nih.gov] […] seizures, and brain atrophy Potassium aggravated myotonia Potato nose Potocki-Lupski syndrome Potocki-Shaffer syndrome Potter sequence PPM-X syndrome Prader-Willi habitus, osteopenia[rarediseases.info.nih.gov] […] syndrome Acrogeria, Gottron type Acrokeratoelastoidosis of Costa Acromegaloid facial appearance syndrome Acromegaloid features, overgrowth, cleft palate and hernia Acromegaloid hypertrichosis[rarediseases.info.nih.gov]

  • Primary Amenorrhea

    All of these features suggested Kallmann syndrome. This syndrome commonly presents with delayed onset of puberty and decreased or absent sense of smell.[ncbi.nlm.nih.gov] Her osteopenia was first diagnosed at the early age of 45 with a lumbar spine bone density T-score of –2.18.[healio.com] Hirsutism and clitoromegaly were present. Ultrasound examination showed polycystic appearance of the ovary.[ncbi.nlm.nih.gov]

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