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同型胱氨酸尿症与晶状体异位。

Homocystinuria and ectopia lentis.

作者信息

Hagee M J

出版信息

J Am Optom Assoc. 1984 Apr;55(4):269-76.

PMID:6609947
Abstract

Homocystinuria is a genetically determined error of metabolism of the amino acid, methionine, which results in increased levels of homocystine and methionine in the blood and urine. A variety of clinical manifestations may result, one of these being the dislocation of the crystalline lens(es). A patient presented in the residency clinic with bilateral ectopia lentis and upon subsequent consultation with her family physician, a diagnosis of homocystinuria was made. This paper discusses the ocular and systemic manifestations of homocystinuria, the differential diagnosis of ectopia lentis, and the management of the systemic disease and its ocular sequelae.

摘要

同型胱氨酸尿症是一种由遗传决定的氨基酸(甲硫氨酸)代谢紊乱疾病,会导致血液和尿液中的同型胱氨酸和甲硫氨酸水平升高。可能会产生多种临床表现,其中之一是晶状体脱位。一名患者在住院诊所就诊时出现双侧晶状体异位,随后在与她的家庭医生会诊后,被诊断为同型胱氨酸尿症。本文讨论了同型胱氨酸尿症的眼部和全身表现、晶状体异位的鉴别诊断以及全身性疾病及其眼部后遗症的治疗。

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