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208 Possible Causes for Androgens Increased, Hirsutism, Kallmann Syndrome

  • Polycystic Ovary Syndrome

    […] or mean follicle number per ovary), whereas only 120 (36%) patients exhibited elevated serum androgens (increased A and/or T concentrations) and 155 (47%) showed elevated[ncbi.nlm.nih.gov] 8 ( FGF8 ) Normosmic hypogonadotrophic hypogonadism and Kallmann syndrome (KAL6) 600483 [612702] Fibroblast growth factor receptor 1 ( FGFR1 ) Kallmann syndrome (KAL2) 136350[ncbi.nlm.nih.gov] Based on results of drug studies on hirsutism, a longer trial of several months may be required to clinically confirm the effects of spearmint tea on hirsutism. 10 In addition[ndnr.com]

  • Hypogonadotropic Hypogonadism

    Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Due to increased androgen accumulation from testosterone, acne may occur.[web.archive.org] Osteoporosis in men has been shown to increase both morbidity and mortality.[omicsonline.org]

  • Achard Thiers Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] Clinical features Achard–Thiers syndrome affects mostly postmenopausal women and comprises diabetes mellitus , deep voice, hirsutism or hypertrichosis , clitoral hypertrophy[ipfs.io] Condition is typically seen in postmenopausal women; cause is hyperplasia of adrenal cortex and increased 11-oxysteroids and androgens. Control is adrenalectomy.[insidesurgery.com]

  • Acquired Adrenogenital Syndrome

    Treatment of a hirsutism presents certain difficulties and is directed to decrease in synthesis of androgens, increase in products of the protein connecting androgens, decrease[en.medicalmed.de] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.de] True hirsutism is distinct from hypertrichosis, which is simply an excessive feminine hair growth.[link.springer.com]

  • Hypogonadism

    SYSTEMIC DISEASES increased SHBG,dec free testosterone Alcohol increases estrogen synthesis Prolactin-supresses FSH,LH Spironolactone(ascites)- supresses androgen CHRONIC[slideshare.net] 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] -Polycystic ovarian syndrome: hirsutism, acne, menstrual disturbances, insulin resistance and, frequently, obesity, form part of this syndrome.[mayomedicallaboratories.com]

  • Placental Aromatase Deficiency

    A dehydroepiandrosterone sulfate loading test induced a marked increase in maternal serum levels of androgens, whereas no such increase was observed in estrogens.[ncbi.nlm.nih.gov] NORMAL testosterone and estrogen levels; thus NORMAL LH Failure to complete puberty Kallmann Syndrome Hypogonadotropic Hypogonadism Defective *migration* of GnRH cells and[quizlet.com] Hirsutism Defined as excessive growth of androgen-responsive terminal hair in women excess hair growth in areas where hair growth is normally minimal Virilization Defined[medbullets.com]

  • HAIR-AN Syndrome

    Increased levels of androgens can also induce symptoms including clitoromegaly, androgenic alopecia, an increased muscle mass and a deep voice.[symptoma.com] […] make-up syndrome Kallmann's syndrome Kanzaki's disease Kasabach-Merritt syndrome Kawasaki's disease KID syndrome Kimura's disease Kindler syndrome Kitamura's reticulate acropigmentation[rr2.nakayamashoten.co.jp] The most common cause of hirsutism is polycystic ovarian syndrome. Patients with "idiopathic" hirsutism have normal ovulatory cycles and androgen levels.[ncbi.nlm.nih.gov]

  • Androgen Therapy

    Such adaptive AR increase paradoxically is a liability in castrated hosts, however, when supraphysiologic androgen is acutely replaced.[ncbi.nlm.nih.gov] Kallmann’s syndrome often includes other abnormalities, such as anosmia and midline cranial defects, colour blindness, deafness and synkinesis.[mja.com.au] Voice change and mild hirsutism were observed in most of the women receiving nandrolone decanoate, and these secondary effects constitute a real disadvantage to its use in[ncbi.nlm.nih.gov]

  • Primary Amenorrhea

    Functional analysis revealed that the mutation induces significantly increased expression of the enzymes involved in androgen biosynthesis (3beta-hydroxysteroid dehydrogenase[ncbi.nlm.nih.gov] 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] Hirsutism and clitoromegaly were present. Ultrasound examination showed polycystic appearance of the ovary.[ncbi.nlm.nih.gov]

  • Patterson Pseudoleprechaunism Syndrome

    Kahrizi syndrome Kaler Garrity Stern Syndrome Kallmann syndrome Kantaputra Gorlin Syndrome Kaplan Plauchu Fitch Syndrome Kaplowitz Bodurtha syndrome Kapur Toriello Syndrome[rgd.mcw.edu] […] adrenal disorder characterized by congenital bronzed hyperpigmentation, cutis laxa of the hands and feet, body disproportion (comprising large hands, feet, nose and ears), hirsutism[orpha.net] […] circulating androgen level ; Intellectual disability, severe ; Joint swelling ; Kyphoscoliosis ; Large hands ; Long foot ; Macrotia ; Metaphyseal sclerosis ; Palmoplantar[mousephenotype.org]

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