A genetic condition where there is an abnormal number of chromosomes, leading to developmental disorders. Early diagnosis matters.
Symptoms vary by condition but may include developmental delays and physical features.
The most common cause is errors during cell division, leading to extra or missing chromosomes.
Prenatal tests like amniocentesis and NIPT help detect aneuploidy early.
Families benefit from genetic counseling and support groups. Get resources for emotional and practical guidance.
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