Undescended testicles, or cryptorchidism, is a condition where one or both of a baby boy’s testicles (testes) have not moved into their proper position in the scrotum by the time of birth. It’s one of the most common disorders of the male genital organs in newborns. Cryptorchidism can affect approximately 1 to 4% of full-term and up to 30% of premature male infants. The condition can involve one (unilateral) or both (bilateral) testicles.
The exact cause of undescended testicles is not fully understood, but it is believed to involve a combination of genetics, maternal health, and environmental factors. Factors that may increase the risk of cryptorchidism include premature birth, low birth weight, family history of the condition, maternal smoking or alcohol use during pregnancy, and conditions of the mother that affect the pregnancy hormones.
The primary symptom of cryptorchidism is the absence of one or both testicles from the scrotum. This can be observed and diagnosed by a physical examination shortly after birth or during infancy.
Cryptorchidism is diagnosed through a physical examination. The doctor may attempt to locate the undescended testicle by palpation (feeling with fingers). If the testicle cannot be felt, additional imaging tests such as ultrasound, MRI, or laparoscopy might be used to locate it.
Treatment for undescended testicles aims to move the testicle into the scrotum and is usually recommended within the first year of life to minimize the risks of infertility and reduce the risk of testicular cancer later in life. Treatment options include:
If left untreated, undescended testicles can lead to several complications later in life, including:
The outlook for boys with undescended testicles is generally excellent, especially when the condition is treated early. Most boys will have normal fertility and sexual function. Regular follow-up into adulthood is recommended for those who have had cryptorchidism, primarily to monitor for signs of testicular cancer.
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