Noun:

হাইপোগোনাডিজম,

hypogonadism শব্দের বাংলা অর্থ এর উদাহরণ:

অন্তর্ভুক্ত লিঊটিয়া ওভারিটিস সিন. উফোরিটিস ওভারিয়ান অবশেষ সিনড্রোম হাইপোগোনাডিজম হাইপারথেকসিস ওভারিয়ান টরসন ওভেরিয়ান অ্যাপপ্লেক্সি (বিচ্ছেদ) অকাল ওভারিয়ান ।

মবিলিটি অস্টিওআর্থারায়টিস লো ব্যাক পেইন মূত্রব্যবস্থা-বিজ্ঞান এবং নেফ্রোলজি ইরেক্টিল ডিসফাংসন মূত্রসংক্রান্ত অসংযম ক্রনিক রেনাল ফাইলইউওর হাইপোগোনাডিজম ।

সবচেয়ে বিশেষভাবে কঙ্কাল পেশীতন্তু মধ্যে. টেসটোসটের সিন্থেটিক ফর্ম হাইপোগোনাডিজম চিকিত্সার জন্য অ্যানাবলিক স্টেরয়েড শুধু এক সাধারণ শ্রেনীর, বিলম্বিত ।

hypogonadism's Usage Examples:

conditions termed hypogonadotropic hypogonadism.

To distinguish it from other forms of hypogonadotropic hypogonadism, Kallmann syndrome has the additional.

Hypogonadotropic hypogonadism (HH), is due to problems with either the hypothalamus or pituitary gland affecting the hypothalamic-pituitary-gonadal axis.

triphenylethylene group which was under development for the treatment of male hypogonadism and type 2 diabetes.

malnutrition, various systemic diseases, or defects of the reproductive system (hypogonadism) or the body's responsiveness to sex hormones.

Hypergonadotropic hypogonadism (HH), also known as primary or peripheral/gonadal hypogonadism, is a condition which is characterized by hypogonadism due to an.

Late-onset hypogonadism (LOH) or Testosterone Deficiency Syndrome (TDS) is a condition in older men characterized by measurably low testosterone levels.

The syndrome is characterized by alopecia, hypogonadism, hypothyroidism, hearing loss, intellectual disability and diabetes mellitus.

Isolated hypogonadotropic hypogonadism (IHH), also called idiopathic or congenital hypogonadotropic hypogonadism (CHH), as well as isolated or congenital.

Defects in this gene are a cause of hypogonadotropic hypogonadism (HH).

clinically as a hormonal therapy in cases of delayed female puberty, hypogonadism, menopausal, and postmenopausal symptoms.

Hormone replacement therapy for people with hypogonadism and intersex conditions (e.

The condition manifests itself as hypergonadotropic hypogonadism (decreased or lack of production of sex steroids by the gonads despite.

which was under development by GlaxoSmithKline for the treatment of hypogonadism (low testosterone levels) in men in the 2000s.

dysfunction Polycystic ovary syndrome (PCOS) Hypogonadotrophic hypogonadism Hypergonadotrophic hypogonadism Tubular dysfunction Pelvic inflammatory disease Endometriosis.

triphenylethylene group that was developed for the treatment of male hypogonadism but was abandoned and never marketed.

sensorineural hearing loss, hair loss associated with pili torti, and hypogonadism demonstrated through low levels of luteinising hormone and growth hormone.

They have clinical applications in the treatment of hypogonadism and infertility.

a cause of hypogonadotropic hypogonadism caused by a luteinizing hormone deficiency.

It is characterized by hypogonadism with spermatogenesis.

The condition manifests itself as isolated hypogonadotropic hypogonadism (IHH), presenting with symptoms such as delayed, reduced, or absent puberty.

Synonyms:

incompetence; Kallman's syndrome; eunuchoidism; male hypogonadism;

Antonyms:

ability; competence;