Last Updated: 8 August 2024
1p36 Deletion Syndrome
Last Updated: 8 August 2024
1p36 Deletion Syndrome
1p36 deletion syndrome is a genetic disorder caused by the deletion of chromosome 1's distal short arm. Symptoms include intellectual disability, developmental delay, seizures, and distinct facial features. Early diagnosis and intervention can improve life quality. 1p36 deletion syndrome affects both sexes equally, with variable symptom severity.
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1p36 Deletion Syndrome
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