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303 Possible Causes for Kallmann Syndrome, Male Hypogonadism, Testicular Disease

  • Kallmann Syndrome

    Signs of reversal may include growth in testicular volume and normalized testosterone levels.[] Kallmann syndrome is the result of a genetic defect.[] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[]

  • Primary Male Hypogonadism

    Classified as primary (resulting from testicular disease), secondary (resulting from pituitary and/or hypothalamic disease), or combined primary/secondary. -- To view the[] Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[] Aim: The creation of new experimental model of primary male hypogonadism.[]

  • Male Hypogonadism

    Hypogonadism may arise from testicular disease (primary hypogonadism) or dysfunction of the hypothalamic-pituitary unit (secondary hypogonadism).[] Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[] In most cases, male hypogonadism is diagnosed through detailed history, physical examination and a few basic hormonal evaluations.[]

  • Hypogonadism

    Hypogonadism is caused by hypothalamic, pituitary, and testicular diseases.[] BACKGROUND: Congenital hypogonadotrophic hypogonadism (CHH) and Kallmann syndrome (KS) are caused by disruption to the hypothalamic-pituitary-gonadal (H-P-G) axis.[] MALE HYPOGONADISM 2.[]

  • Anorchia

    From Wikidata Jump to navigation Jump to search human disease Testicular agenesis Bilateral anorchia edit Language Label Description Also known as English Anorchia human disease[] Conditions associated with hypogonadotropic hypogonadism Kallmann syndrome Anosmia (lack of sense of smell) or hyposmia is a prominent feature of Kallmann syndrome, which[] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[]

  • Cryptorchidism

    Cryptorchidism can therefore be considered a symptom of impaired testicular function that may also be linked to other testicular diseases, such as germ cell cancer and subfertility[] Whereas the duplication mutation has not been reported before, p.Pro26Leu was once observed in a Kallmann syndrome patient.[] Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. Andrology. 2013; 1:3-16. 18.[]

  • Testicular Atrophy

    Testicular atrophy is a disease that results in the decrease of testicular size.[] Kallmann syndrome has been described in both familial (X-linked and autosomal) and sporadic forms, and its incidence is estimated as 1 case per 30,000 male births and 1 per[] Male hypogonadism occurs when a man's testicles cannot produce adequate levels of testosterone. According to Northwestern Memorial Hospital urologist, Dr.[]

  • Luteinizing Hormone Deficiency

    The measurement of LH and FSH may differentiate between benign symptoms and true disease.[] This disorder featuring lack of sense of smell is called anosmia or Kallmann syndrome.[] LH mediated high intra-testicular testosterone is essential for postnatal male sexual maturation and spermatogenesis.[]

  • Kallmann Syndrome Type 4

    […] the absence of hypothalamic, pituitary or testicular disease. 5 There are gaps in the evidence base in relation to the potential benefits of testosterone treatment in men[] Kallmann syndrome can have a wide variety of additional signs and symptoms.[] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[]

  • Hypogonadotropic Hypogonadism Type 21

    It can be due to a testicular disorder or the result of a disease process involving the hypothalamus and pituitary gland.[] […] a b c d e f g h i "Kallmann syndrome".[] Testicular adrenal rest tumors develop independently of long-term disease control: a longitudinal analysis of 50 adult men with congenital adrenal hyperplasia due to classic[]

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