Prenatal diagnosis of multiple acyl-CoA dehydrogenase deficiency: Association with elevated α-fetoprotein and cystic renal changes

Prenatal Diagnosis

Volumn 21, Issue 10, 2001, Pages 856-859

  Chisholm, Christian A ^a   Vavelidis, Fotini ^a   Lovell, Mark A ^a   Sweetman, Lawrence ^a   Roe, Charles R ^a   Roe, Diane S ^b   Frerman, Frank E ^c   Wilson, William G ^a  

^a UNIVERSITY OF VIRGINIA   (United States)

^b BAYLOR UNIVERSITY MEDICAL CENTER   (United States)

^c Children's Hospital Colorado   (United States)

Author keywords

fetoprotein; Counseling; Cystic renal disease; Organic aciduria; Prenatal diagnosis

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; ACYLCARNITINE; ALPHA FETOPROTEIN;

ARTICLE; CAUCASIAN; ECHOGRAPHY; ENZYME DEFICIENCY; FATTY LIVER; FETUS; FIRST TRIMESTER PREGNANCY; HUMAN; INTRAUTERINE GROWTH RETARDATION; KIDNEY CYST; OLIGOHYDRAMNIOS; PATIENT COUNSELING; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASES; ALPHA-FETOPROTEINS; AMNIOCENTESIS; AMNIOTIC FLUID; CARNITINE; DIAGNOSIS, DIFFERENTIAL; FATTY LIVER; FEMALE; FETAL DISEASES; FETAL GROWTH RETARDATION; GESTATIONAL AGE; HUMANS; OLIGOHYDRAMNIOS; POLYCYSTIC KIDNEY DISEASES; PREGNANCY; PRENATAL DIAGNOSIS; ULTRASONOGRAPHY, PRENATAL;

EID: 0035164490     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.157     Document Type: Article

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