CRIPAK

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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.