Prevalence and Incidence of Cri-du-chat syndrome
Prevalance of Cri-du-chat syndrome:
1 per 200,000-500,000 newborns are affected by Cri-du-chat syndrome, Genetics Home Reference website ... see also overview of Cri-du-chat syndrome.
Prevalance Rate:
approx 1 in 200,000 or 0.00% or 1,360 people in USA [Source statistic for calcuation: "1 per 200,000-500,000 newborns are affected by Cri-du-chat syndrome, Genetics Home Reference website" -- see also general information about data sources]
Cri-du-chat syndrome: Rare Disease
Cri-du-chat syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Cri-du-chat syndrome, or a subtype of Cri-du-chat syndrome,
affects less than 200,000 people in the US population.
Ophanet, who are a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Cri-du-chat syndrome as a "rare disease".
More information about Cri-du-chat syndrome is available from Orphanet
About prevalence and incidence statistics:
The term 'prevalence' of Cri-du-chat syndrome usually refers to the estimated population
of people who are managing Cri-du-chat syndrome at any given time.
The term 'incidence' of Cri-du-chat syndrome refers to the annual diagnosis rate,
or the number of new cases of Cri-du-chat syndrome diagnosed each year.
Hence, these two statistics types can differ:
a short-lived disease like flu can have high annual incidence but low prevalence,
but a life-long disease like diabetes has a low annual incidence but high prevalence.
For more information see about prevalence and incidence statistics.
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