Mucopolysaccharidosis type VII as a cause of recurrent non-immune hydrops fetalis

Journal of Perinatal Medicine

Volumn 31, Issue 6, 2003, Pages 535-537

  Cheng, Yvonne ^a   Verp, Marion S ^a   Knutel, Terri ^a   Hibbard, Judith U ^a  

^a UNIVERSITY OF CHICAGO   (United States)

Author keywords

Hydrops fetalis; Mucopolysacchariodosis VII; Prenatal diagnosis

Indexed keywords

BETA GLUCURONIDASE;

ADULT; ARTICLE; BETA GLUCURONIDASE DEFICIENCY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; ENZYME DEFICIENCY; FEMALE; FETUS; FETUS HYDROPS; HUMAN; LYSOSOME STORAGE DISEASE; MUCOPOLYSACCHARIDOSIS TYPE 7; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RECURRENT DISEASE;

ADULT; FEMALE; FETAL DEATH; GESTATIONAL AGE; HETEROZYGOTE DETECTION; HUMANS; HYDROPS FETALIS; MUCOPOLYSACCHARIDOSIS VII; PREGNANCY; PREGNANCY COMPLICATIONS; ULTRASONOGRAPHY, PRENATAL;

EID: 0346963112     PISSN: 03005577     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPM.2003.083     Document Type: Article

References (8)

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