XK aprosencephaly: An extremely rare condition where the forebrain is absent as well as other abnormalities. More detailed information about the symptoms, causes, and treatments of XK aprosencephaly is available below.
See full list of 11 symptoms of XK aprosencephaly
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Read more about Misdiagnosis and XK aprosencephaly
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XK aprosencephaly is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that XK aprosencephaly, or a subtype of XK aprosencephaly,
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 XK aprosencephaly as a "rare disease".
Source - Orphanet
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