Kozlowski-Brown-Hardwick syndrome: A very rare syndrome characterized mainly by various skeletal anomalies, unusual facial appearance, eye abnormalities and communicating hydrocephaly. More detailed information about the symptoms, causes, and treatments of Kozlowski-Brown-Hardwick syndrome is available below.
See full list of 12 symptoms of Kozlowski-Brown-Hardwick syndrome
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Kozlowski-Brown-Hardwick syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Kozlowski-Brown-Hardwick syndrome, or a subtype of Kozlowski-Brown-Hardwick syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Kozlowski-Brown-Hardwick syndrome as a "rare disease".
Source - Orphanet
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