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860 Possible Causes for Hirsutism, Hypothyroidism, Kallmann Syndrome

  • Polycystic Ovary Syndrome

    The purpose of the study is to examine the impact of subclinical hypothyroidism on the characteristics of PCOS patients.[] 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[]

  • Acquired Adrenogenital Syndrome

    The authors also investigate the diseases of the neurohypophysis and of the thyroid such as diabetes insipidus, hypernatraemia (salt imbalance), hypothyroidism, myxedema coma[] 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.[]

  • Primary Amenorrhea

    No similar observation has been reported earlier in juvenile hypothyroidism.[] 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.[]

  • Hypogonadotropic Hypogonadism

    The first patient presented congenital hypogonadotropic hypogonadism combined with mild central hypothyroidism and growth hormone deficiency occurred in the peripubertal age[] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[] […] dwarfism (-4 SD) and Tanner stage P0 G1 was identified together with low IGF-1 and non-stimulated growth hormone after insulin stimulation; also secondary adrenal insufficiency hypothyroidism[]

  • Secondary Amenorrhea

    Kallmann syndrome most commonly occurs as an X-linked recessive disorder caused by a KAL1 defect.[] […] e.g., eating disorder, excessive exercise, hyperandrogenism, visual defects, vaginal dryness, and hot flashes physical examination e.g., body mass index, acne, hirsutism,[] These two adolescent girls thus appear to have isolated hypothalamic hypothyroidism.[]

  • Galactorrhea-Amenorrhea Syndrome

    May occur in dogs with severe hypothyroidism, due to hyperprolactinemia, pseudocyesis, or trauma to the mammary gland.[] Identification of one or more mutations in a member of the KAL gene family confirms a diagnosis of Kallmann’s syndrome.[] المحتويات Diethylstilbestrol 159 Adnexal Masses 183 Hirsutism 199 Contraception 213 Infertility 236 Menopause 256 Evaluation of Sexual Dysfunction 275 Sexual Harassment Sexual[]

  • Primary Hypergonadotropic Hypogonadism-Partial Alopecia Syndrome

    Hypothyroidism and Myxedema Coma Iodine Deficiency Lithium-Induced Goiter Medullary Thyroid Carcinoma Myxedema Coma or Crisis Neurological Manifestations of Thyroid Disease[] Isolated Adrenal Insufficiency Due To Partial Cyp11A1 Deficiency Insulin-Resistance Syndrome Type A Kallmann Syndrome Laron Syndrome Leopard Syndrome 1 Leptin Receptor Deficiency[] Blood and urine tests can help evaluate the cause of hirsutism. Treatment is aimed at slowing new hair growth.[]

  • Hypogonadism

    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.[] ‘Medical disorders such as Cushing's syndrome, hypothyroidism and hypogonadism rarely cause obesity.’ Pronunciation hypogonadism /ˌhʌɪpə(ʊ)ˈɡəʊnadɪz(ə)m[]

  • Achard Thiers Syndrome

    Includes: athyroidism (acquired) hypothyroidism (acquired) myxedema (adult) (juvenile) thyroid (gland) insufficiency (acquired) 244.0 Postsurgical hypothyroidism 244.1 Other[] 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[]

  • Hypopituitarism

    Antithyroid antibodies, in the normal range three months postpartum, became significantly elevated when the hypothyroidism appeared.[] syndrome Lymphocytic hypophysitis Transsphenoidal adenomectomy Congenital - Usually presents in childhood, but can present later with features such as delayed puberty; heritable[] Plasma testosterone binding globulin and indexes of the concentration of unbound androgens in normal and hirsute subjects. J Clin Endocrinol Metab 1971; 32:717. 33.[]

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