小兒科CHEN, CHIH-PINGCHIH-PINGCHENLIN, SHUAN-PEISHUAN-PEILINTZEN, CHIN-YUANCHIN-YUANTZENHWU, WUH-LIANGWUH-LIANGHWUCHERN, SCHU-RERNSCHU-RERNCHERNWANG, WAY-SEENWAY-SEENWANG2008-12-052018-07-112008-12-052018-07-112007http://ntur.lib.ntu.edu.tw//handle/246246/88661We present prenatal diagnosis of mucopolysaccharidosis type II (MPS II) ( Hunter syndrome) and demonstrate marked mucopolysaccharide deposition in multiple vital organs in a 22-gestational-week affected fetus. Level II ultrasound showed cardiomegaly and hepatomegaly. Histological examinations of the fetal vital organs manifested marked mucopolysaccharide deposition . We suggest that any therapeutic approach and counseling for prenatally diagnosed MPS II should consider the early signs of in utero marked mucopolysaccharide storage.en-USHunter syndromemucopolysaccharide depositionMucopolysaccharidosis type IIprenatal diagnosistherapyjournal article