Postnatal molecular karyotyping is a modern genetic test that provides accurate detection of chromosomal changes in children (and adults)
The test examines deletions and duplications of small regions of the chromosome, which are often impossible to detect with classical karyotyping.
Array CGH Molecular cytogenetic research method that combines Comparative Genomic Hybridization (CGH) Technique and Microarray To use
Postnatal molecular karyotyping is recommended for children who have:
– Developmental delay
– Congenital defects
– Suspicion of genetic syndromes
The study is also conducted in adults who:
– Have a history of infertility or recurrent miscarriages
– Neurological disorders (which sometimes appear later)
– Developmental and intellectual disabilities and others
Postnatal molecular karyotyping (array CGH)
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