Opitz G/BBB Syndrome: A rare genetic disorder characterized by defects along the midline of the body. The type and severity of symptoms can vary considerably. There are two subtypes of the disorder: one is inherited in a X-linked manner and the other is inherited in an autosomal dominant manner. Females with the X-linked form of the condition tend to have few symptoms and often only have wide set eyes. More detailed information about the symptoms, causes, and treatments of Opitz G/BBB Syndrome is available below.
See full list of 33 symptoms of Opitz G/BBB Syndrome
See full list of 6 treatments for Opitz G/BBB Syndrome
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Prognosis for Opitz G/BBB Syndrome: The prognosis varies depending on the type and severity of the symptoms which can vary considerably amongst patients. Prognosis and quality of life can be improved by appropriate treatment and monitoring. Most patients have a normal life span and normal growth.
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