Edward Syndrome with Aplasia Cutis Congenita: A Rare Case Report
Aplasia cutis congenita (ACC) is a rare developmental malformation characterized by the absence of skin, extending to bone or dura in a localized or widespread area at birth. Mostly it's seen in the scalp with an autosomal dominant inheritance and slight female predisposition. Generally, it is...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
JCDR Research and Publications Pvt. Ltd.,
2014-07-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |