Isodicentric 15

Isodicentric 15 (also known as idic(15), partial tetrasomy 15q, or inverted duplication 15) is a genetic disorder caused by the presence of an extra chromosome 15, or part of it, which is mirrored on both sides of the centromere. This condition is a type of chromosomal abnormality known as a chromosome duplication.

Symptoms and Signs[edit | edit source]

The symptoms of Isodicentric 15 can vary widely among affected individuals. Common symptoms include intellectual disability, developmental delay, autism spectrum disorder, seizures, and behavioral problems. Some individuals may also have physical abnormalities such as unusual facial features, short stature, and skeletal abnormalities.

Causes[edit | edit source]

Isodicentric 15 is caused by a duplication of a portion of chromosome 15. This duplication occurs during the formation of reproductive cells (meiosis) or in early embryonic development. The exact reason why this duplication occurs is not known.

Diagnosis[edit | edit source]

Diagnosis of Isodicentric 15 is typically made through genetic testing, which can identify the presence of the extra chromosome 15. This testing can be done through blood tests, amniocentesis, or chorionic villus sampling.

Treatment[edit | edit source]

There is currently no cure for Isodicentric 15. Treatment is focused on managing the symptoms and improving the quality of life for affected individuals. This may include physical therapy, occupational therapy, speech therapy, and behavioral therapy. Medications may also be used to manage seizures and other symptoms.

References[edit | edit source]

Isodicentric 15 Resources
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