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Carey Fineman Ziter syndrome (medical condition): A rare inherited disorder characterized by nonprogressive muscle weakness from birth as well as the Moebius (congenital facial palsy with impaired ability to move eyes) and Pierre Robin sequence (underdeveloped jaw, cleft soft palate, abnormal tongue position).
See also:
Myopathy, congenital nonprogressive with Moebius and Robin sequences:
»Introduction: Myopathy, congenital nonprogressive with Moebius and Robin sequences
»Symptoms of Myopathy, congenital nonprogressive with Moebius and Robin sequences
Carey Fineman Ziter syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Carey Fineman Ziter syndrome, or a subtype of Carey Fineman Ziter 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 if affects 1 person per 2,000.
They list Carey Fineman Ziter syndrome as a "rare disease".
Source - Orphanet
Carey Fineman Ziter syndrome: Another name for Myopathy, congenital nonprogressive with Moebius and Robin sequences (or close medical condition association).
»Introduction: Myopathy, congenital nonprogressive with Moebius and Robin sequences
»Symptoms of Myopathy, congenital nonprogressive with Moebius and Robin sequences
Some of the symptoms of Carey Fineman Ziter syndrome incude:
Source - NIH
Source: Diseases Database
Search to find out more about Carey Fineman Ziter syndrome:
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