Fetal polycystic kidney disease associated with glutaric aciduria type II: An inborn error of energy metabolism

American Journal of Perinatology

Volumn 13, Issue 3, 1996, Pages 130-134

  Whitfield, Jonathan ^a   Hurst, David ^a   Bennett, Michael J ^a   Sherwood, W Geoff ^a   Hogg, Ronald ^a   Gonsoulin, Whitney ^a  

^a BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Hyperechoic; Multiple acyl CoA dehydrogenase defect; Polycystic

Indexed keywords

ACIDURIA; AMINO ACID METABOLISM; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; FETUS; GENETIC COUNSELING; HUMAN; KIDNEY POLYCYSTIC DISEASE; PRIORITY JOURNAL;

ACYL-COA DEHYDROGENASES; ADULT; AMINO ACID METABOLISM, INBORN ERRORS; DIAGNOSIS, DIFFERENTIAL; FATTY ACIDS; FEMALE; FETAL DISEASES; GENES, RECESSIVE; GLUTARATES; HUMANS; INFANT, NEWBORN; POLYCYSTIC KIDNEY DISEASES; PREGNANCY; ULTRASONOGRAPHY, PRENATAL;

EID: 0029874136     PISSN: 07351631     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-994309     Document Type: Article

References (15)

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