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C Syndrome: A rare inherited disorder characterized by a triangular-shaped head, facial anomalies, joint contractures and loose skin. More detailed information about the symptoms, causes, and treatments of C Syndrome is available below.
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A multiple congenital anomaly/mental retardation syndrome marked by trigonocephaly due to craniosynostosis, orofacial anomalies (mainly metopic prominence, upward slating of the palpebral fissures, epicanthal folds, hypoplastic nose, malformed ears, and abnormal palate) associated with various renal, pulmonary, genital, and cardiovascular defects. Agenesis of the corpus callosum and tetralogy of Fallot in some cases. Opitz trigonocephaly and Varadi-Papp syndromes have many common characteristics. - (Source - Diseases Database)
C Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that C Syndrome, or a subtype of C Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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