Gyrate atrophy is autosomal recessive dystrophy in which night blindness starts in the first decade of life. Peripheral field loss usually begins in the second and third decades as the disease progresses. There is no gender predilection. It is commoner in Finland (1/50,000).

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Inborn Errors of Metabolism: Gyrate Atrophy

  • Kristina J. Hartung,
  • Stephen H. Tsang,
  • Tarun Sharma,
  • Vlad Diaconita

摘要

Gyrate atrophy is autosomal recessive dystrophy in which night blindness starts in the first decade of life. Peripheral field loss usually begins in the second and third decades as the disease progresses. There is no gender predilection. It is commoner in Finland (1/50,000).