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Medical condition/treatment
Cri-du-chat syndrome
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Hole body
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Cri-du-chat syndrome is a genetic disorder characterized by a characteristic cat-like cry in infants, developmental delays, intellectual disability, and distinctive facial features. It is caused by a deletion on chromosome 5.
Causes/Description:
Cri du chat syndrome is a genetic disorder caused by a deletion on chromosome 5. The exact cause of this deletion is unknown, but genetics plays a role. Other factors may include environmental factors and neural wiring disorders.
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Physiotherapie, Ergotherapie, Logopädie, Frühintervention, Entwicklungsförderung, Familientherapie, Psychologische Unterstützung, Selbsthilfegruppen
50 min
260 Swiss francs
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Cri du chat syndrome is caused by a deletion on the short arm of chromosome 5. This deletion occurs randomly and can result in the disorder's characteristic features, including a high-pitched, shrill cry similar to a cat's meow.
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- Early intervention and early intervention - Speech and communication therapy - Behavior management and social skills training - Physiotherapy to improve mobility - Family training and support
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Cri du chat syndrome was first described by J. Lejeune in 1963. It is a rare genetic disorder caused by the missing part of the short arm of chromosome 5. Characteristic features include a high-pitched shrill cry in infancy, facial deformities, developmental delays and intellectual disabilities. Treatment focuses on managing symptoms and supporting development.
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