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MeSH 搜索器

Aicardi Syndrome

A rare genetic disorder characterized by partial or complete absence of the CORPUS CALLOSUM, resulting in infantile spasms, MENTAL RETARDATION, and lesions of the RETINA or OPTIC NERVE.
推出的年份: 2011
副标题
树号: C10.500.034.687, C11.270.019, C16.131.162, C16.131.666.034.687, C16.320.290.019, C16.320.322.030
MeSH 单一 ID: D058540
进入的组:
  • Syndrome, Aicardi
  • Corpus Callosum, Agenesis Of, With Chorioretinal Abnormality
  • Chorioretinal Anomalies with Acc
  • Agenesis of Corpus Callosum with Infantile Spasms and Ocular Abnormalities
  • Callosal Agenesis and Ocular Abnormalities
  • Aicardi's Syndrome
  • Syndrome, Aicardi's
  • Agenesis of Corpus Callosum with Chorioretinal Abnormality
早前的内容:
  • Syndrome (1972-2010)

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