Computer-based facial recognition as an assisting diagnostic tool to identify children with Noonan syndrome
Abstract Background Noonan syndrome (NS) is a rare genetic disease, and patients who suffer from it exhibit a facial morphology that is characterized by a high forehead, hypertelorism, ptosis, inner epicanthal folds, down-slanting palpebral fissures, a highly arched palate, a round nasal tip, and po...
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| Huvudupphov: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Utgiven: |
BMC
2024-05-01
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| Serie: | BMC Pediatrics |
| Ämnen: | |
| Länkar: | https://doi.org/10.1186/s12887-024-04827-7 |
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