3q29 microdeletion syndrome

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A genetic disorder caused by a deletion on chromosome 3





3q29 microdeletion syndrome is a rare genetic disorder characterized by a deletion of a small segment of chromosome 3 at the q29 band. This condition can lead to a variety of developmental and health issues, including intellectual disability, developmental delay, and distinctive facial features.

Genetics[edit | edit source]

The 3q29 microdeletion syndrome is caused by the deletion of a segment of DNA on the long arm (q arm) of chromosome 3. This deletion typically spans approximately 1.6 million base pairs and affects multiple genes. The deletion is usually de novo, meaning it occurs as a new mutation in the affected individual and is not inherited from the parents.

Clinical Features[edit | edit source]

Individuals with 3q29 microdeletion syndrome may present with a range of clinical features, which can vary in severity. Common features include:

Diagnosis[edit | edit source]

Diagnosis of 3q29 microdeletion syndrome is typically made using chromosomal microarray analysis, which can detect the deletion of the 3q29 region. Karyotyping may also be used, but it is less sensitive for detecting small deletions.

Management[edit | edit source]

There is no cure for 3q29 microdeletion syndrome, and management focuses on addressing the specific symptoms and needs of the individual. This may include:

  • Early intervention programs for developmental delays
  • Special education services
  • Behavioral therapy for autism spectrum disorder
  • Regular monitoring and treatment of associated health issues

Prognosis[edit | edit source]

The prognosis for individuals with 3q29 microdeletion syndrome varies depending on the severity of symptoms and the presence of associated health conditions. With appropriate support and interventions, many individuals can lead fulfilling lives.

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Gallery[edit | edit source]

3q29 microdeletion syndrome[edit | edit source]

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Contributors: Prab R. Tumpati, MD