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Chromosome Microdeletions, Molecular Detection

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Chromosome Microdeletions, Molecular Detection

Accredited Facility E-report Qualified Specialists

This molecular genetic test identifies small chromosomal deletions (microdeletions) that may not be visible on conventional chromosome analysis. It helps diagnose genetic syndromes, developmental disorders, and congenital conditions.

  • If a genetic syndrome is suspected.
  • During evaluation of developmental delay or intellectual disability.
  • When congenital abnormalities are present.
  • If there is a family history of chromosomal disorders.
  • As part of genetic counseling and diagnostic assessment.
  • No fasting is usually required.
  • A blood sample or other genetic specimen may be collected.
  • Genetic counseling may be recommended before and after testing.
  • Inform the healthcare provider about personal and family medical history.
  • Follow all laboratory instructions before sample collection.
    • Chromosome Microdeletions, Molecular Detection
    No labs currently offering this test.