Congenital microcephaly detected by prenatal ultrasound: Genetic aspects and clinical significance

Ultrasound in Obstetrics and Gynecology

Volumn 15, Issue 4, 2000, Pages 282-287

  Den Hollander, N S ^a   Wessels, M W ^a   Los, F J ^a   Ursem, N T C ^a   Niermeijer, M F ^a   Wladimiroff, J W ^a  

^a ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

Genetic counselling; Heterogeneity; Microcephaly; Prenatal diagnosis; Ultrasound

Indexed keywords

ARTICLE; BRAIN MALFORMATION; CHROMOSOME DISORDER; CLINICAL ARTICLE; DIAGNOSTIC IMAGING; FETUS; FETUS ECHOGRAPHY; GENETIC COUNSELING; HEAD CIRCUMFERENCE; HOLOPROSENCEPHALY; HUMAN; MICROCEPHALY; MULTIPLE MALFORMATION SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; ULTRASOUND;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; FEMALE; GESTATIONAL AGE; HUMANS; KARYOTYPING; MICROCEPHALY; PREGNANCY; RETROSPECTIVE STUDIES; SYNDROME; ULTRASONOGRAPHY, PRENATAL;

EID: 0034544876     PISSN: 09607692     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1469-0705.2000.00092.x     Document Type: Article

References (11)

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5. Ultrasound criteria for in utero diagnosis of microcephaly
6. The diagnosis of fetal microcephaly
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8. Ultrasonic measurement of the fetal abdominal circumference in estimation of fetal weight
9. Monochorionic twin pregnancies: Les liaisons dangereuses
10. Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection
11. Prenatal diagnosis of microcephaly assisted by vaginal sonography and power Doppler