Clinical Features of Apert Syndrome in Infancy: A rare case in Indonesia
Background: Apert syndrome is characterized by several malformations of cranial-facial and syndactyly. The incidence of Apert syndrome was reported at approximately 1 per 65,000 live births, globally. Fibroblast Growth Factor 2 (FGFR2) is believed to hold a key role in the syndrome. Objectives: Th...
Furkejuvvon:
| Váldodahkkit: | , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Talenta Publisher
2021-02-01
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| Ráidu: | Scripta Score Scientific Medical Journal |
| Fáttát: | |
| Liŋkkat: | https://talenta.usu.ac.id/scripta/article/view/4563 |
| Fáddágilkorat: |
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