Thompson Syndrome 1
General: Autosomal dominant inheritance.
Ocular: Congenital optic atrophy; nystagmus; blindness.
Clinical: None.
Magalini SI, Scrascia E. Dictionary of Medical Syndromes, 2nd ed. Philadelphia: JB Lippincott, 1981.
Thompson AH, Cashell GTW A pedigree congenital optic atrophy entrancing sixteen affected cases in six generations. Proc R Soc Med 1935; 28:1415-l426.
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