Understanding the Condition
What is Male Hypogonadism?
Dr Syed Kazmi, Consultant Endocrinologist at Naas Cardiology & Endocrinology Clinic in Naas, Co. Kildare (IMC 213626), provides specialist assessment and management of this condition. Appointments are available on Saturdays and Sundays at Suite 5, Vista Primary Care Clinic, Ballymore Road, Naas. To book, call 089 656 7597.
Male hypogonadism is a clinical syndrome resulting from failure of the testes to produce adequate levels of testosterone, sperm, or both. It is classified by the level at which the failure occurs:
Primary hypogonadism (hypergonadotrophic) results from testicular failure — the testes do not respond normally to hormonal stimulation from the pituitary. Causes include Klinefelter syndrome, previous chemotherapy or radiotherapy, mumps orchitis, or cryptorchidism.
Secondary (hypogonadotrophic) hypogonadism results from insufficient pituitary or hypothalamic stimulation of the testes. Causes include pituitary tumours, haemochromatosis, obesity, opioid use, and idiopathic hypogonadotrophic hypogonadism.
Distinguishing between these types requires specialist assessment and directs appropriate treatment.
This page is for educational purposes only. It does not constitute medical advice. Always consult a qualified healthcare professional for assessment and management of suspected testosterone deficiency.