CRIPAK
Cripak: A Comprehensive Guide to a Rare Genetic Disorder
Description:
Cripak, also known as Cri-du-chat syndrome, is a rare genetic condition caused by a deletion of part or all of chromosome 5. This deletion results in a characteristic high-pitched cry in infancy, which gives the syndrome its name. Cripak affects multiple systems of the body, leading to developmental delays, intellectual disability, and physical abnormalities.
Associated Diseases:
- Intellectual disability
- Delayed speech and language development
- Autism spectrum disorder
- Heart defects
- Kidney malformations
- Feeding difficulties
- Growth retardation
Did you Know ?
Cripak occurs in approximately 1 in every 50,000 live births worldwide.
