新生儿筛查
入射(几何)
粘多糖病
干血
I型粘多糖病
医学
亨特综合征
粘多糖病Ⅱ型
儿科
人口
Hurler综合征
内科学
疾病
酶替代疗法
化学
色谱法
物理
光学
环境卫生
作者
Barbara K. Burton,Vera P. Shively,Allegra Quadri,Lauren Warn,Jennifer Burton,Dorothy K. Grange,Katherine Christensen,Daniel Groepper,Laura Ashbaugh,Joan Ehrhardt,Khaja Basheeruddin
标识
DOI:10.1016/j.ymgme.2023.107557
摘要
We describe our experience with population-based newborn screening for mucopolysaccharidosis type II (MPS II) in 586,323 infants by measurement of iduronate-2-sulfatase activity in dried blood spots between December 12, 2017 and April 30, 2022. A total of 76 infants were referred for diagnostic testing, 0.01% of the screened population. Of these, eight cases of MPS II were diagnosed for an incidence of 1 in 73,290. At least four of the eight cases detected had an attenuated phenotype. In addition, cascade testing revealed a diagnosis in four extended family members. Fifty-three cases of pseudodeficiency were also identified, for an incidence of 1 in 11,062. Our data suggest that MPS II may be more common than previously recognized with a higher prevalence of attenuated cases.
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