Create issue ticket

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[] 8 ( FGF8 ) Normosmic hypogonadotrophic hypogonadism and Kallmann syndrome (KAL6) 600483 [612702] Fibroblast growth factor receptor 1 ( FGFR1 ) Kallmann syndrome (KAL2) 136350[] 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[]

  • Hypogonadotropic Hypogonadism

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

  • Achard Thiers Syndrome

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

  • 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[] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[] True hirsutism is distinct from hypertrichosis, which is simply an excessive feminine hair growth.[]

  • Hypogonadism

    SYSTEMIC DISEASES increased SHBG,dec free testosterone Alcohol increases estrogen synthesis Prolactin-supresses FSH,LH Spironolactone(ascites)- supresses androgen CHRONIC[] BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[] -Polycystic ovarian syndrome: hirsutism, acne, menstrual disturbances, insulin resistance and, frequently, obesity, form part of this syndrome.[]

  • 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.[] NORMAL testosterone and estrogen levels; thus NORMAL LH Failure to complete puberty Kallmann Syndrome Hypogonadotropic Hypogonadism Defective *migration* of GnRH cells and[] 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[]

  • HAIR-AN Syndrome

    Increased levels of androgens can also induce symptoms including clitoromegaly, androgenic alopecia, an increased muscle mass and a deep voice.[] […] 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[] The most common cause of hirsutism is polycystic ovarian syndrome. Patients with "idiopathic" hirsutism have normal ovulatory cycles and androgen levels.[]

  • Androgen Therapy

    Such adaptive AR increase paradoxically is a liability in castrated hosts, however, when supraphysiologic androgen is acutely replaced.[] Kallmann’s syndrome often includes other abnormalities, such as anosmia and midline cranial defects, colour blindness, deafness and synkinesis.[] 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[]

  • Primary Amenorrhea

    Functional analysis revealed that the mutation induces significantly increased expression of the enzymes involved in androgen biosynthesis (3beta-hydroxysteroid dehydrogenase[] All of these features suggested Kallmann syndrome. This syndrome commonly presents with delayed onset of puberty and decreased or absent sense of smell.[] Hirsutism and clitoromegaly were present. Ultrasound examination showed polycystic appearance of the ovary.[]

  • Patterson Pseudoleprechaunism Syndrome

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

Similar symptoms