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431 Possible Causes for Gynecomastia, Kallmann Syndrome, Male Hypogonadism

  • Hypogonadism

    Additional features suggest specific disorders, eg, anosmia in Kallmann syndrome; eunuchoid body habitus, gynecomastia, and small testes in Klinefelter syndrome.[mdedge.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] MALE HYPOGONADISM 2.[slideshare.net]

  • Kallmann Syndrome

    We report a case of Kallmann syndrome that presented with delay puberty, color blindness, gynecomastia, and absence of smell.[ncbi.nlm.nih.gov] Kallmann syndrome is the result of a genetic defect.[symptoma.com] Causes Male hypogonadism means the testicles don't produce enough of the male sex hormone testosterone. There are two basic types of hypogonadism: Primary.[mayoclinic.org]

  • Primary Male Hypogonadism

    Increase oestrogen effect on breast tissue What are the causes of gynecomastia?[brainscape.com] Secondary hypogonadism can be caused by Kallmann syndrome, pituitary or hypothalamic tumors or disorders, obesity, diabetes and Prader-Willi syndrome.[froedtert.com] Aim: The creation of new experimental model of primary male hypogonadism.[ingentaconnect.com]

  • Male Hypogonadism

    Since gynecomastia is a prominent clinical manifestation in patients with 17-ketosteroid reductase deficiency after puberty, 2,9-11 we suspected that some men with gynecomastia[nejm.org] Disorders Causing Pituitary Hypogonadism Brain and pituitary tumors Hemochromatosis Kallmann syndrome Weight loss Obesity Diabetes Testicular Disorders Causing Hypogonadism[louisville.edu] In most cases, male hypogonadism is diagnosed through detailed history, physical examination and a few basic hormonal evaluations.[ncbi.nlm.nih.gov]

  • Hypogonadotropic Hypogonadism

    REIFENSTEIN, FULLER ALBRIGHT, Syndrome Characterized by Gynecomastia, Aspermatogenesis without A-Leydigism, and Increased Excretion of Follicle-Stimulating Hormone, The Journal[oadoi.org] Patients with Kallmann's syndrome or idiopathic hypogonadotropic hypogonadism usually have absent puberty.[endobible.com] Abstract Male hypogonadism is defined as the deficiency of testosterone or sperm production synthesized by testicles or the deficiency of both.[ncbi.nlm.nih.gov]

  • Anorchia

    Enlarge Print Diagnosis of Gynecomastia Figure 1. Algorithm for the diagnosis of gynecomastia. Diagnosis of Gynecomastia Figure 1.[aafp.org] Conditions associated with hypogonadotropic hypogonadism Kallmann syndrome Anosmia (lack of sense of smell) or hyposmia is a prominent feature of Kallmann syndrome, which[emedicine.medscape.com] Gynecomastia How can you classify male hypogonadism into 3 types? memorize this 1.[quizlet.com]

  • Hypogonadotropic Hypogonadism Type 8

    Phenotypes Anosmia ; Autosomal recessive inheritance ; Azoospermia ; Cryptorchidism ; Decreased testicular size ; Delayed skeletal maturation ; Gonadotropin deficiency ; Gynecomastia[mousephenotype.org] Schlüsselwörter Kallmann-Syndrom - hypogonadotroper Hypogonadismus - Anosmie - Genetik Keywords Kallmann’s syndrome - hypogonadotropic hypogonadism - anosmia - genetics[thieme-connect.com] Male hypogonadism that occur secondary to hypothalamic-pituitary dysfunction is known as hypogonadotropic hypogonadism (HH).[dnatesting.uchicago.edu]

  • Klinefelter Syndrome

    Gynecomastia is treated surgically because of the potential danger of malignancy or for cosmetic reasons.[oadoi.org] All patients with Kallmann syndrome required long term testosterone treatment.[ncbi.nlm.nih.gov] Male Hypogonadism. p. 367. CrossRef Google Scholar Amory, John K. and Bremner, William J. 2017. Male Hypogonadism . p. 187.[doi.org]

  • Hypogonadotropic Hypogonadism Type 22

    Signs and symptoms may include: Erectile dysfunction Infertility Decrease in beard and body hair growth Decrease in muscle mass Development of breast tissue (gynecomastia)[mayoclinic.org] Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005;25:98–9. PubMed Crossref Google Scholar 3.[degruyter.com] Case Report : The patient was a 30-year-old male who presented with complaints of failure to attain puberty, break in voice, gynecomastia, marfanoid features, under developed[atmph.org]

  • Cryptorchidism

    Whereas the duplication mutation has not been reported before, p.Pro26Leu was once observed in a Kallmann syndrome patient.[ncbi.nlm.nih.gov] Male hypogonadism: an extended classification based on a developmental, endocrine physiology-based approach. Andrology. 2013; 1:3-16. 18.[revistas.uis.edu.co] […] of hypogonadism and a harbinger of adult reproductive dysfunction ( Grumbach 2005 ; Main et al. 2000, 2006b ; Suomi et al. 2006 ).[doi.org]

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