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Opitz-Kaveggia syndrome (medical condition): A rare genetic disorder characterized by anal abnormalities,...more »
See also:
FG Syndrome:
»Introduction: FG Syndrome
»Symptoms of FG Syndrome
Opitz-Kaveggia syndrome: A multiple congenital anomaly/mental retardation syndrome characterized by a short stature, large head, hypotonia with or without joint contractures, seizures, imperforate anus, agenesis of the corpus callosum, and characteristic facies. "FG" stands for the surnames of patients in whom the syndrome was first reported.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Opitz-Kaveggia syndrome:
Opitz-Kaveggia syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Opitz-Kaveggia syndrome, or a subtype of Opitz-Kaveggia syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Opitz-Kaveggia syndrome: Another name for FG Syndrome (or close medical condition association).
»Introduction: FG Syndrome
»Symptoms of FG Syndrome
Opitz-Kaveggia syndrome: Opitz-Kaveggia syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Opitz-Kaveggia syndrome incude:
See full list of 46 symptoms of Opitz-Kaveggia syndrome (FG Syndrome)
These medical disease topics may be related to Opitz-Kaveggia syndrome:
Source: Diseases Database
Source - NIH
Source: Diseases Database
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