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925 Possible Causes for Hirsutism, Kallmann Syndrome

  • Hypogonadotropic Hypogonadism

    Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Quinton R (ed): Kallmann Syndrome and Hypogonadotropic Hypogonadism. Front Horm Res.[karger.com] Overview What is Kallmann Syndrome?[thinkgenetic.com]

  • Polycystic Ovary Syndrome

    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] Context: Hirsutism often occurs in women with polycystic ovary syndrome (PCOS).[ncbi.nlm.nih.gov]

  • Hypogonadism

    Polycystic ovary syndrome, and Kallmann syndrome, also called hypogonadotropic hypogonadism. Hemochromatosis and diabetes mellitus can be causes of this as well.[en.wikipedia.org] -Polycystic ovarian syndrome: hirsutism, acne, menstrual disturbances, insulin resistance and, frequently, obesity, form part of this syndrome.[mayomedicallaboratories.com] […] baseline free testosterone concentrations was very well tolerated and did not result in adverse events, including lipid or liver abnormalities or significant differences in hirsutism[healio.com]

  • 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[the-medical-dictionary.com] Clinical features Achard–Thiers syndrome affects mostly postmenopausal women and comprises diabetes mellitus , deep voice, hirsutism or hypertrichosis , clitoral hypertrophy[ipfs.io]

  • Multicentric Osteolysis-Nodulosis-Arthropathy Spectrum

    PROKR2) Kallmann syndrome 3 KAL4 (offiz. PROK2) Hypogonadism, hypogonadotropic Kallmann syndrome 4 KAL5 (off.[uniklinik-freiburg.de] Additional features include coarse face, corneal opacities, patches of thickened, hyperpigmented skin, hypertrichosis and gum hypertrophy.[malacards.org] Coarse face and body hirsutism are additional features.[ncbi.nlm.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] Hirsutism and clitoromegaly were present. Ultrasound examination showed polycystic appearance of the ovary.[ncbi.nlm.nih.gov] Patients with primary amenorrhea, hirsutism, and gonadotropic abnormalities should be evaluated for hyperandrogenemia.[clinicaladvisor.com]

  • Acquired Adrenogenital Syndrome

    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] 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]

  • HAIR-AN Syndrome

    […] 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] The most common cause of hirsutism is polycystic ovarian syndrome. Patients with “idiopathic” hirsutism have normal ovulatory cycles and androgen levels.[doi.org]

  • Lytic Bone Lesion

    , see ophthalmo-acromelic syndrome anosmic hypogonadism, see Kallmann syndrome anosmic idiopathic hypogonadotropic hypogonadism, see Kallmann syndrome ANS, see ataxia neuropathy[mygenomics.com] SFPKS was first described in a 5-year-old female with a distinct facial appearance, proportional short stature, hirsutism, polycystic kidneys, vertebral abnormalities, elongated[nature.com] hypertrichosis / Increased body hair - Hyperextensible joints / articular hyperlaxity - Hypoplastic mandibula / partial absence of the mandibula - Macrocephaly / macrocrania[csbg.cnb.csic.es]

  • Sertoli Leydig Cell Tumor

    ジュベー症候群 MarieJoubert Canadian neurologist Kahn カーン Kahn test カーンテスト Kallmann カルマン Kallmann syndrome カルマン症候群 Kaposi カポジ Kaposi's sarcoma カポジ肉腫 Móric Kaposi (1837 -1902) Hungarian[jams.med.or.jp] The patient was alive and well with improved hirsutism 4 years after the operation.[ncbi.nlm.nih.gov] Hirsutism acne, oily skin, increased libido, virilization 1. Clitoromegaly 2. Deepening of voice 3. Balding 4.[brainscape.com]

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