XYY syndrome

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(Redirected from XYY Karyotype)

Genetic condition affecting males with an extra Y chromosome


XYY syndrome
Synonyms 47,XYY syndrome, Jacob's syndrome, XYY karyotype
Pronounce N/A
Field Medical genetics, Pediatrics
Symptoms Tall stature, learning difficulties, delayed speech and language skills, behavioral challenges
Complications N/A
Onset Congenital (present from birth)
Duration Lifelong
Types N/A
Causes Nondisjunction leading to an extra Y chromosome
Risks N/A
Diagnosis Karyotype analysis, prenatal diagnosis via amniocentesis or chorionic villus sampling
Differential diagnosis N/A
Prevention N/A
Treatment Supportive; may include speech therapy, occupational therapy, behavioral therapy, and educational support
Medication N/A
Prognosis Generally good with supportive care
Frequency ~1 in 1,000 male births
Deaths N/A


XYY syndrome, also known as 47,XYY syndrome, Jacob's syndrome, or simply XYY karyotype, is a genetic disorder in which a male individual possesses an extra Y chromosome, resulting in a total of 47 chromosomes instead of the typical 46. The condition is caused by a random error known as nondisjunction during the formation of sperm cells and is not typically inherited.

Amniocentesis showing a 47,XYY karyotype

Overview[edit | edit source]

Males with XYY syndrome have the chromosomal pattern 47,XYY, as opposed to the typical male karyotype of 46,XY. This chromosomal difference usually occurs spontaneously and is not associated with environmental or parental risk factors. The extra Y chromosome is present in every cell of the body and can result in various physical, developmental, and behavioral features.

Signs and Symptoms[edit | edit source]

Many individuals with XYY syndrome may not exhibit noticeable symptoms and remain undiagnosed. However, some common characteristics include:

Despite these challenges, intelligence is typically within the normal range, though some may have slightly lower than average IQ scores.

Causes[edit | edit source]

XYY syndrome arises from a random event during the process of meiosis in sperm cell development. Specifically, nondisjunction results in a sperm cell containing two Y chromosomes instead of one. When this sperm fertilizes a normal egg, the resulting embryo has an XYY karyotype.

This genetic condition is not inherited and is usually considered a sporadic or de novo chromosomal abnormality.

Diagnosis[edit | edit source]

Diagnosis of XYY syndrome can occur at different life stages:

In many cases, individuals may remain undiagnosed due to the often mild or absent symptoms.

Treatment and Management[edit | edit source]

There is no specific cure for XYY syndrome, as it is a chromosomal condition. Management is individualized and supportive, focusing on addressing specific needs:

Some individuals may also benefit from psychological evaluation and support to manage social anxiety, emotional regulation, or self-esteem issues.

Prognosis[edit | edit source]

The prognosis for individuals with XYY syndrome is generally favorable. With early identification and supportive interventions, most individuals lead healthy, productive lives. They are capable of attending regular schools, pursuing higher education, maintaining employment, and leading independent lives.

Fertility is typically normal, and there is no increased risk of passing on the condition to offspring beyond the general population risk.

Epidemiology[edit | edit source]

XYY syndrome is estimated to occur in approximately 1 in 1,000 live male births. Due to the mild presentation in many cases, it is believed that a significant number of individuals remain undiagnosed throughout their lives.

Misconceptions[edit | edit source]

Historical misconceptions suggested a link between XYY syndrome and increased aggression or criminal behavior. These theories have been largely discredited. Most individuals with XYY are not more likely to exhibit antisocial behavior than the general population.

Related Conditions[edit | edit source]

See also[edit | edit source]


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Contributors: Prab R. Tumpati, MD