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Arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones
  1. P. A. Bhaskar,
  2. K. Jagannathan,
  3. K. Valmikinathan
  1. Institute of Neurology, Government General Hospital, Madras-3, India

    Abstract

    Two male cousins are reported with arachnodactyly, selective aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones, and a distant female relative with similar abnormalities. The syndrome is thought to be previously undescribed, though it has resemblances to Marinesco-Sjögren and Marfan's syndromes.

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