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Six cases of Edward syndrome who were born at Cheil Hospital was presented.
These babies had grossly multiple anomalies that were characterized by promint occiput,
micrognathia, small palpebral fissures, small oral opening, narrow high palatal arch, low set ear, overlapping fingers, prominent labia minora and majora, narrow pelvis, and Rocker bottom feet.
We have been confirmed by chromosome culture and their chromosomal analysis... |
