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A doctor may then order testing to see … 47 XYY Syndrome Treatment This condition cannot be corrected but to prevent the occurrence of this syndrome on the patient's posterity, it is best that genetic testing must be done. This is just the result of an accidental event during sperm cell formation. The most characteristic feature of XYY Syndrome is that the affected individual will be extremely tall. The primary features are infertility and small poorly functioning testicles. Boys with XYY syndrome — also known as 47,XYY — might be taller than other boys. In fact, with early intervention and treatment, the problems associated with this rare chromosomal disorder can be … XYY syndrome treatment.

About 1 in 1,000 boys have it.

XYY syndrome is a sex chromosome abnormality in which boys are born with two Y chromosomes and one X chromosome. .

47 XYY syndrome: Introduction. If you or your son is diagnosed with Klinefelter syndrome, your health care team may include a doctor who specializes in diagnosing and treating disorders involving the body's glands and hormones (endocrinologist), a speech therapist, a pediatrician, a physical therapist, a genetic counselor, a reproductive medicine or infertility specialist, and a counselor or psychologist. In majority of the cases of XYY Syndrome, the affected individuals will have severe acne while in their teenage years.

A blood test can also accurately diagnose XYY syndrome. 47 XYY Syndrome Causes 47 XYY syndrome is not an inherited condition. Often, symptoms may be subtle and many people do not realize they are affected. The most characteristic feature of XYY Syndrome is that the affected individual will be extremely tall.
47 XYY syndrome: A genetic condition where males have an extra Y chromosome in each of their cells. Despite the fact that 1 in 1000 boys 1-6 have the karyotype 47,XYY (XYY), there is a paucity of information about the phenotype, and approximately 85% or more of males with XYY are never diagnosed. 47,XYY syndrome is associated with an increased risk of learning disabilities and delayed development of speech and language skills. Genes contain instructions that determine how the body is supposed to function. Normally male cells have one X and one Y chromosome. What is XYY syndrome? Since it's impossible to correct every sex chromosome in our bodies, there is no treatment for XYY syndrome. Tall stature is a characteristic feature. Spencer DA, Eyles JW, Mason MK. Objective To investigate the criminal pattern in men between 15 and 70 years of age diagnosed with 47,XXY (Klinefelter's syndrome (KS)) or 47,XYY compared to the general population. XYY syndrome (1:1000 live births) The 47,XYY syndrome results from parental nondisjunction during meiosis, resulting in an extra Y chromosome. The signs and symptoms of XYY syndrome can be managed with a variety of therapies.

The Syndrome XYY does not affect the life expectancy of a person at all.

J Med Genet. Males with this condition experience normal sexual development, however, there may be an increased risk of developmental delays in speech, language, motor, or behavioral abilities. XYY syndrome is a genetic condition found in males only. [PMC free article] Swerdlow AJ, Schoemaker MJ, Higgins CD, Wright AF, Jacobs PA. Cancer incidence and mortality in men with Klinefelter syndrome: A cohort study.
Occupational therapy may be recommended for infants and young boys who have low muscle tone (hypotonia), and speech therapy may be recommended for boys who have speech delay. Most XYY men are fertile; however, there is a subset of men who show severe oligospermia or azoospermia.