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Arthrogryposis multiplex congenita - pulmonary hypoplasia: A rare congenital syndrome involving degeneration of the brain and spinal cord and characterized by facial, head, skeletal and muscular abnormalities. Reduced fetal activity causes many of the problems. More detailed information about the symptoms, causes, and treatments of Arthrogryposis multiplex congenita - pulmonary hypoplasia is available below.
See full list of 36 symptoms of Arthrogryposis multiplex congenita - pulmonary hypoplasia
Review possible medical complications related to Arthrogryposis multiplex congenita - pulmonary hypoplasia:
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Prognosis for Arthrogryposis multiplex congenita - pulmonary hypoplasia: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
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