Apert syndrome with glucose-6-phosphate dehydrogenase deficiency: a case report
Apert syndrome is characterized by midface hypoplasia, syndactyly of the hands and feet, proptosis of eyes,steep and flat frontal bones, and premature union of cranial sutures.
| Main Author: | G. TOSUN & Y. SENER |
|---|---|
| Format: | Koleksi Audio Visual |
| Language: | Bahasa Inggris |
| Published: |
Paediatric Dentistry
2006
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| Subjects: | |
| Online Access: |
http://oaipmh-jogjalib.umy.ac.idkatalog.php?opo=lihatDetilKatalog&id=94252 |