β-glucuronidase deficiency as cause of recurrent hydrops fetalis: The first early prenatal diagnosis by chorionic villus sampling

Prenatal Diagnosis

Volumn 18, Issue 9, 1998, Pages 959-962

  Van Eyndhoven, H W F ^a,d   Ter Brugge, H G ^a   Van Essen, A J ^b   Kleijer, W J ^c  

^a HOSPITAL DE WEEZENLANDEN   (Netherlands)

^b UNIVERSITY OF GRONINGEN   (Netherlands)

^c ERASMUS MEDICAL CENTER   (Netherlands)

^d MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Hydrops fetalis; Mucopolysaccharidosis type VII; Prenatal diagnosis

Indexed keywords

BETA GLUCURONIDASE;

ADULT; ARTICLE; CASE REPORT; CHORION VILLUS SAMPLING; ENZYME DEFICIENCY; FEMALE; FETUS HYDROPS; HUMAN; MUCOPOLYSACCHARIDOSIS TYPE 7; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ADULT; AMNIOCENTESIS; CELLS, CULTURED; CHORIONIC VILLI; CHORIONIC VILLI SAMPLING; DISEASES IN TWINS; FEMALE; FIBROBLASTS; GESTATIONAL AGE; GLUCURONIDASE; HUMANS; HYDROPS FETALIS; MALE; PREGNANCY; RECURRENCE; ULTRASONOGRAPHY, PRENATAL;

EID: 0031725688     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199809)18:9<959::AID-PD372>3.0.CO;2-I     Document Type: Article

References (12)

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