Genetic syndromes and prenatally detected renal anomalies

Seminars in Fetal and Neonatal Medicine

Volumn 13, Issue 3, 2008, Pages 171-180

  Deshpande, C ^a   Hennekam, R C M ^b,c,d  

^a GUY S HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^d ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

Antenatal ultrasound scan; Chromosome anomaly; Genetic syndromes; Oligohydramnios; Renal agenesis; Renal cysts; Renal enlargement; Teratogenicity

Indexed keywords

ARTICLE; BARDET BIEDL SYNDROME; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; CONGENITAL DISORDER OF GLYCOSYLATION; CONGENITAL MALFORMATION; ECHOGRAPHY; ELLIS VAN CREVELD SYNDROME; FRYNS SYNDROME; GENETIC DISORDER; HUMAN; HYDRAMNIOS; INBORN ERROR OF METABOLISM; JEUNE SYNDROME; JOUBERT SYNDROME; KIDNEY AGENESIS; KIDNEY HYPERTROPHY; KIDNEY MALFORMATION; KIDNEY POLYCYSTIC DISEASE; MARDEN WALKER SYNDROME; MECKEL SYNDROME; OLIGOHYDRAMNIOS; PERLMAN SYNDROME; PIERSON SYNDROME; PRENATAL DIAGNOSIS; SIMPSON GOLABI BEHMEL SYNDROME; SMITH LEMLI OPITZ SYNDROME; TERATOGENESIS; ZELLWEGER SYNDROME;

BECKWITH-WIEDEMANN SYNDROME; CHROMOSOME ABERRATIONS; FEMALE; FETUS; GENETIC DISEASES, INBORN; HUMANS; KIDNEY; OLIGOHYDRAMNIOS; POLYHYDRAMNIOS; PREGNANCY; PREGNANCY TRIMESTER, SECOND; PRENATAL DIAGNOSIS; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 41549143371     PISSN: 1744165X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.siny.2007.10.006     Document Type: Article

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