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,其中最常以渐进性水晶体异位呈现。
Conclusion: Homocystinuria is a rare autosomal-recessive disorder with multiple systemic complications.Progressive myopia and ectopia lentis are common presenting signs in such patients.
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,其中最常以渐进性水晶体异位呈现。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件观点;若发现问题,欢迎向我们指正。
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,其中最常以渐进性近视及水晶体异位。
明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发
问题,欢迎向我们指正。
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遗传疾病,可导致多样全
症,其中最常以渐进
近视及水晶体异位呈现。
声明:以上例句、词分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件
观点;若
现问题,欢迎向我们指正。
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,其中最常以渐进性近视及水晶体异位。
明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发
问题,欢迎向我们指正。
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,其中最常以渐进性近视及水晶体异。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发问题,欢迎向我们指正。
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,其中最常渐进性近视及水晶体异位呈现。
声:
例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
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
以渐进性近视及水晶体异位呈现。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
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,可样全身并发症,其中最常以渐进性
视及水晶体异位呈现。
声明:以上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。
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。
声明:上例句、词性分类均由互联网资源自动生成,部分未经过人工审核,其表达内容亦不代表本软件的观点;若发现问题,欢迎向我们指正。