Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.
高胱胺酸尿症为一少见之体染色体隐性遗传疾病,可导致多样全身并发症,其中最

进性近视及水晶体
位呈现。
位(器官等的位置
,
是先天性的)
,反
,变态,畸形;

况;Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.
高胱胺酸尿症为一少见之体染色体隐性遗传疾病,可导致多样全身并发症,其中最

进性近视及水晶体
位呈现。
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