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2,920 Possible Causes for Hemoglobin Decreased, Kallmann Syndrome, Mutation in the KISS1 Receptor Gene

  • Hypogonadotropic Hypogonadism

    […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Subnormal testosterone is not related to glycosylated hemoglobin or duration of diabetes.[endocrineweb.com]

  • Male Hypogonadism

    gene (KISS1 receptor product)?[quizlet.com] Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[louisville.edu] Physical abilities in hypogonadal men are further hampered by lower oxygen supply due to decreased hemoglobin concentrations and by poor glucose utilization.[ncbi.nlm.nih.gov]

  • Primary Male Hypogonadism

    gene (KISS1 receptor product)?[quizlet.com] Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[froedtert.com] Treatment of Kallmann syndrome with hCG can correct cryptorchidism and establish fertility. Puberty is typically induced using testosterone injectable or gel.[merckmanuals.com]

  • Hypogonadotropic Hypogonadism Type 8

    Mutations involving the genes GnRH1 and KISS1, are a very rare cause of HH [41], [42].[journals.plos.org] Symptoms were present for 2 – 9 months before endocrine evaluation; and were attributed to the “iron overload, chronic diseases itself, low hemoglobin level, liver dysfunction[mjhid.org] Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[thieme-connect.com]

  • Hypogonadism

    […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] It is even thought to decrease insulin resistance improve glycemic control, cholesterol levels, and hemoglobin A1C.[symptoma.com] 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]

  • Kallmann Syndrome Type 3

    gene (KISS1 receptor product)?[quizlet.com] Subnormal testosterone is not related to glycosylated hemoglobin or duration of diabetes.[endocrineweb.com] […] a b c d e f g h i "Kallmann syndrome".[en.wikipedia.org]

  • Kallmann Syndrome Type 4

    […] in the genes encoding GNRH1 or its receptor will result in the failure of the HPG axis and give rise to normosmic CHH. [2] Inactivating mutations of KISS1 or KISS1R causes[en.wikipedia.org] Subnormal testosterone is not related to glycosylated hemoglobin or duration of diabetes.[endocrineweb.com] Kallmann syndrome can have a wide variety of additional signs and symptoms.[ghr.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism Type 18

    […] identified two novel missense mutations in the gene encoding the GNRH receptor ( GNRHR1 : NM_000406.2; HGNC: 4421), see Figure 2 .[journals.plos.org] syndrome", abstract "The genetic basis is unknown for 60{\%} of normosmic hypogonadotropic hypogonadism (nHH)/Kallmann syndrome (KS).[augusta.pure.elsevier.com] Symptoms were present for 2 – 9 months before endocrine evaluation; and were attributed to the “iron overload, chronic diseases itself, low hemoglobin level, liver dysfunction[mjhid.org]

  • Hypocupremia

    Ceruloplasmin and copper-zinc SOD are decreased in copper deficiency, affecting the survival of erythrocytes.[haematologica.org] Additional features suggest specific disorders, eg, anosmia in Kallmann syndrome; eunuchoid body habitus, gynecomastia, and small testes in Klinefelter syndrome.[mdedge.com] Congenital secondary hypogonadism Congenital secondary hypogonadism results from isolated gonadotropin deficiency due to genetic mutations, such as Kallmann syndrome, Prader–Willi[dermnetnz.org]

    Missing: Mutation in the KISS1 Receptor Gene
  • Cronkhite-Canada Syndrome

    Hypophosphatasia 140 Weaver Syndrome 19 Kallmann Syndrome 141 WeillMarchesani Syndrome 20 Laron Dwarfism 142 WeismannNetterStuhl Syndrome 21 Lipodystrophy Acquired Generalized[books.google.ro] 15 Growth Hormone Deficiency 137 Triploidy SyndromePartial Molar Pregnancy 16 HAIRAN Syndrome 138 Turner Syndrome 17 Hermaphroditism True 139 Von HippelLindau Disease 18[books.google.ro] Thrombocytopenia and Absent Radius Syndrome 12 Carcinoid Syndrome 134 Tooth Agenesis Anodontia 13 Cushing Syndrome 135 TownesBrocks Syndrome 14 Diabetes Insipidus 136 TreacherCollins Syndrome[books.google.ro]

    Missing: Mutation in the KISS1 Receptor Gene

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