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早产儿家族性X-连锁低磷性佝偻病1例报道 被引量:1

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摘要 X-连锁低磷性佝偻病(X-linked hypophOSphatemic rickets,XLH)是最常见的遗传性佝偻病,发病率为1∶12 000,占家族性低磷性佝偻病的80%以上。多数于婴儿期后发病,表现为身材矮小、骨骼畸形,血生化改变为低磷血症、碱性磷酸酶活性增高等。该病的遗传方式为X-连锁显性遗传。
出处 《中国儿童保健杂志》 CAS 2017年第8期863-864,共2页 Chinese Journal of Child Health Care
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