학술저널
Marfan`s syndrome is a collagenous hereditary disorder characterized by skeletal defects, cardiovascular defects and ocular defects. Recently, authors experienced two cases of Marfan`s syndrome with 10year old girl and 30 year old man. In both cases, the characteristic findings were lenticular dislocation with coloboma and opacity, visual disturbance, elongation of long bone, fingers and toes. The clinical findings, the result of surgical treatment & brief review of literature were reported as follows.
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