PIGMENTARY DEGENERATION OF THE RETINA IN THE HALLERVORDEN-SPATZ SYNDROME

Dizygotic twins developed a progressive neurologic disorder at age 6 months. When examined at age 7 1 2 years each had spastic quadriparesis and dystonia. Neither had ever spoken a complete sentence. The fundi showed bone spicule formation, a conspicuous choroidal circulation, and a striking accumulation of yellowish-white globular masses of varying sizes and shapes. Because our patients developed both the pigmentary degeneration and clinical signs of Hallervorden-Spatz syndrome at a much younger age than patients without retinopathy, we believe this case demonstrated a distinct nosologic entity. © 1979.