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49 Possible Causes for Glucose Tolerance Test Abnormal, Hirsutism, Kallmann Syndrome

  • Polycystic Ovary Syndrome

    Once the diagnosis was made, she was screened for lipid abnormalities and for glucose intolerance.[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]

  • Achard Thiers Syndrome

    Because affected women are hyperinsulinemic, a two-hour oral glucose tolerance test shows abnormally elevated levels of glucose in the blood.[rarediseases.org] 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]

  • Acquired Adrenogenital Syndrome

    AGS Adrenogenital syndrome AGT alanine-glyoxylate amniotransferase AGTT Abnormal glucose tolerance test AGU Anhydroglucose Units AGUS Atypical glandular cells of uncertain[globalrph.com] 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]

  • Primary Amenorrhea

    If impaired (fasting glucose 100–125 mg/dL), patients should undergo an oral glucose tolerance test.[clinicaladvisor.com] 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]

  • HAIR-AN Syndrome

    In these instances, a glucose tolerance test may be necessary to reveal the underlying abnormality of insulin resistance. 2 To evaluate the possibility of hyperandrogenism[aafp.org] […] 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]

  • Carney Complex

    […] blood test results of high insulin-like growth factor 1 (IGF-I) levels, abnormal glucose tolerance test (GTT), and/or paradoxical growth hormone (GH) response to thyrotropin-releasing[cancer.net] Syndrom MLL2 Kallmann-Syndrom KAL1, FGFR1, CHD7, FGF8, PROK2, PROKR2, KISS1R, GNRHR kongenitales zentrales Hypoventilationssyndrom PHOX2B Lamelläre Ichtyosis ABCA12, TGM1[meduniwien.ac.at] Abstract A woman with Carney complex presented at the age of 22 years with abdominal pain and hirsutism.[ncbi.nlm.nih.gov]

  • Amaurosis-Hypertrichosis Syndrome

    glucose tolerance, TG and elevated LDL:HDL ratio 47.[slideshare.net] […] of lacrimal and salivary glands) FGF23 (Hypophosphatemic rickets, autosomal dominant) FGF3 (Deafness, congenital with inner ear agenesis, microtia, and microdontia) FGF8 (Kallmann[en.praenatal-medizin.de] MalaCards based summary : Amaurosis Congenita, Cone-Rod Type, with Congenital Hypertrichosis, is also known as amaurosis congenita cone-rod type with congenital hypertrichosis[malacards.org]

  • Rabson Mendenhall Syndrome

    Of the remainder of patients, about 50% will show abnormalities when challenged by routine or cortisone glucose tolerance tests.[telemedicine.org] Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.com] Rabson-Mendenhall syndrome is characterized by growth retardation, dysmorphisms, lack of subcutaneous fat, acanthosis nigricans, enlarged genitalia, hirsutism, premature and[ncbi.nlm.nih.gov]

  • Hypopituitarism

    At age 17 months hypoglycemic seizures occured (blood glucose 5 mg/100 ml). An oral glucose tolerance test was abnormal.[pediatrics.aappublications.org] syndrome Lymphocytic hypophysitis Transsphenoidal adenomectomy Congenital - Usually presents in childhood, but can present later with features such as delayed puberty; heritable[emedicine.com] 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.[medtextfree.wordpress.com]

  • Congenital Isolated ACTH Deficiency

    Abnormal glucose tolerance test results are present in most patients.[glowm.com] Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of: · gonadotropin · growth hormone · pituitary hormone Kallmann's syndrome Lorain-Levi[apps.who.int] Content Clinical Overview Diagnosis Indications for Testing Ambiguous genitalia or unexplainable electrolyte results in infancy Premature sexual development in older children Hirsutism[arupconsult.com]

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