Last Updated: 8 August 2024
16p12.2 Microdeletion
Last Updated: 8 August 2024
16p12.2 Microdeletion
The 16p12.2 microdeletion is a rare genetic disorder involving the loss of a small segment of chromosome 16. This deletion can lead to developmental delays, intellectual disabilities, and various physical and behavioural abnormalities. Diagnosis is through genetic testing, and management typically involves supportive therapies tailored to individual needs.
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16p12.2 Microdeletion
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