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KMID : 0374919930140020317
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Inje Medical Journal
1993 Volume.14 No. 2 p.317 ~ p.322
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A Case of Holoprosencephaly
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Abstract
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Holoprosencephaly is the result of an embryogenic defect of prechodal mesoderm which leads to incomplete morphogenesis of the fore brain and variable deficit of facial midline anomalies.
A case of holoprosencephaly, alobal type with premaxillary agenesis in 1-day-female patient was presented. She had hypotelorism, cleft upper lip, and flat nasal bridge. Diagnosis of holoprosencephaly is confirmed by clinical features and CT-scan.
A
brief review of literatures was made.
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KEYWORD
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