Cri-du-Chat Syndrome

Overview

An infantile syndrome characterized by a cat-like cry, failure to thrive, microcephaly, MENTAL RETARDATION, spastic quadriparesis, micro- and retrognathia, glossoptosis, bilateral epicanthus, hypertelorism, and tiny external genitalia. It is caused by a deletion of the short arm of chromosome 5 (5p-).

This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.

Quick facts about Cri-du-Chat Syndrome

Topic type

Condition

Category

Neurology

MeSH classification

C10.597.606.360.180|C16.131.077.262|C16.131.260.190|C16.320.180.190

Preparing for an appointment about Cri-du-Chat Syndrome

If you are speaking with a healthcare professional about Cri-du-Chat Syndrome, it can help to prepare a few details in advance.

• Write down your symptoms and when they started.
• Bring details of any medicines, supplements or previous treatments.
• Ask what tests or assessments may be needed.
• Ask what treatment or management options may be suitable.
• Ask when you should seek urgent medical help or follow-up care.

Finding care related to Cri-du-Chat Syndrome

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