Apert syndrome with lobar holoprosencephaly and agenesis of corpus callosum in a Palestinian neonate: case report
Full term female newborn was a product of normal delivery, she had dysmorphic feature ;small eye sockets,proptosis,hypertelorism,down slanted palpebral fissure, low set ears, depressed nose bridge, narrow high arched palate, trapezoid mouth, bilateral hands had complex syndactyly involving 2nd ,3rd...
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| Format: | Article |
| Language: | English |
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Bulgarian Association of Young Surgeons
2019-03-01
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| Series: | International Journal of Medical Reviews and Case Reports |
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| Online Access: | http://www.ejmanager.com/fulltextpdf.php?mno=299473 |