Kallman's syndrome is a disorder of hypogonadotropic hypogonadism, delayed puberty, and anosmia (the inability to smell). Kallman's syndrome is a birth defect in the brain that prevents release of hormones and appears as failure of male puberty. Some boys have adequate amounts of androgen in their system but fail to respond to them, a condition known as androgen resistance. Hypogonadotropic hypogonadism (hh) occurs when the body does not produce enough of two important hormones, luteinizing hormone (lh) and follicle stimulating hormone (fsh). This results in underdeveloped gonads and often infertility. Anosmia, the inability to smell, was first described with hypogonadotropic hypogonadism in 1856, but it was not until 1944 that an instance of kallman's reported the inheritance of the two symptoms together in three separate families.

Last week, we started a topic on male hypogonadism. We discussed the definition, types andsomecauses. This week, we will continue with some of the primary and secondary causes of male hypogonadism and few signs and symptoms. Hemochromatosis:this condition is characterized by excess of iron in the bloodstream. Hemoglobin, which is composed of both the heme (iron) and the globulin (protein) parts, is often the main component of the red blood cell. Too much iron in the blood may eventually cause the pituitary gland or the testicles to stop functioning properly, which may reduce the amount of testosterone that is produced. https://www.tumblr.com/blog/survivormaleenhancers https://www.reverbnation.com/survivormaleenhancement

How common is male hypogonadism?

2. Definition male hypogonadism is a clinical syndrome caused by androgen deficiency which may adversely affect multiple organ functions and quality of life. Sources: guidelines on male hypogonadism. European association of urology 2015. Nieschlag e, et al. Andrology: male reproductive health and dysfunction. 3rd edn. Springer-verlag berlin heidelberg 2010 isbn 978-3-540-78354-1 3. Secondary rabi’atul ‘adawiyah binti mohamad 10-6-76 4. Kallmann syndrome. Gnrh deficiency with anosmia disorders hyperprolactinemia inflammatory disease sarcoidosis, histiocytosis and tuberculosis hiv/aids medications obesity normal aging concurrent illness 5. Pathogenesis dhamirah sakinah binti makmon 10-6-75 6. Clinical picture ahmad naufal b nordeen 10-6-16 siti aisyah bt ahmad faizal 10-6-85 siti khadijah bt mansor 10-6-89 siti zulaikha bt saian 10-6-90 7. Primary hypogonadism secondary hypogonadism genetic: klinefelter’s syndrome (common) congenital: anorchia kallman syndrome pituitary gland tumor 8. Klinefelter’s syndrome

The Testis and Male Sexual Function

what is it? it is a condition in which the male hormone testosterone is not produced at levels that are necessary to meet the body’s demand for appropriate function. This is a medical condition that is widely underdiagnosed. Why is this condition underdiagnosed? this condition is underdiagnosed because of the following frank reasons: men do not like to go to the physician men do not like to complain about their symptoms to their primary physician most of the symptoms associated with this condition are very vague to be recognized by the individual as a “medical condition” most men are discreet about their lack of sexual function or performance.

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In women ( ovaries ovaries ovaries are the paired gonads of the female reproductive system that contain haploid gametes known as oocytes. The ovaries are located intraperitoneally in the pelvis, just posterior to the broad ligament, and are connected to the pelvic sidewall and to the uterus by ligaments. These organs function to secrete hormones (estrogen and progesterone) and to produce the female germ cells (oocytes). Ovaries: anatomy ): lh lh a major gonadotropin secreted by the adenohypophysis. Luteinizing hormone regulates steroid production by the interstitial cells of the testis and the ovary. The preovulatory luteinizing hormone surge in females induces ovulation, and subsequent luteinization of the follicle. https://survivormaleenhancers.company.site