Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.
结论：高胱胺
为一少见之体染色体隐性遗传疾病，可导致多样全身并发，其中最常以
进性近视及水晶体异位呈现。
Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.
结论：高胱胺为一少见之体染色体隐性遗传疾病，可导致多样全身并发，其中最常以进性近视及水晶体异位呈现。
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