A Case of Holoprosencephaly / 대한산부인과학회잡지
Korean Journal of Obstetrics and Gynecology
;
: 2035-2038, 2002.
Article
in Korean
| WPRIM
| ID: wpr-114673
ABSTRACT
Holoprosencephaly is a rare developmental defect due to incomplete cleavages of the prosencephalon during the third week of fetal development. It was associated with chromosomal anomalies, genetic syndrome, teratogen, or genetic disorder of non-syndromic HPE. Early antenatal detection of holoprosencephaly was done by high resolution ultrasonography. According to its severity and prognosis, it was capable of proper treatment of holoprosencephaly. We report one case of holoprosencephaly with a brief review of the literature
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Prognosis
/
Holoprosencephaly
/
Ultrasonography
/
Prosencephalon
/
Fetal Development
Type of study:
Diagnostic study
/
Prognostic study
Language:
Korean
Journal:
Korean Journal of Obstetrics and Gynecology
Year:
2002
Type:
Article
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