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2022 临床实践指南：布罗索尤单抗时代儿童X-连锁低磷血症的治疗

2022-04-15 澳大利亚皇家医师学院 J Paediatr Child Health

儿童X-连锁低磷血症布罗索尤单抗

X-连锁低磷血症（XLH）是最常见的遗传性低磷血症。致病基因是位于X染色体上与内肽酶同源的磷酸盐调节基因(PHEX基因),呈显性遗传。本文主要针对儿童XLH应用布罗索尤单抗治疗提供指导建议。

中文标题：

2022 临床实践指南：布罗索尤单抗时代儿童X-连锁低磷血症的治疗

英文标题：

Clinical practice guidelines for paediatric X-linked hypophosphataemia in the era of burosumab

发布机构：

澳大利亚皇家医师学院

发布日期：

2022-04-15

简要介绍：

X-连锁低磷血症（XLH）是最常见的遗传性低磷血症。致病基因是位于X染色体上与内肽酶同源的磷酸盐调节基因(PHEX基因),呈显性遗传。本文主要针对儿童XLH应用布罗索尤单抗治疗提供指导建议。

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    2022-07-11 一名医生👩‍⚕️

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    2022-04-19 doctor.huang1907

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