Pierre Robin sequence and keratoconus, a rare association
Pierre Robin sequence (PRS) is an inherited disorder that affects one in between 8,500 and 14,000 people and is characterized by a triad of clinical signs. These include micrognathia, glossoptosis and obstruction of the upper airway, typically associated with palatal cleft. PRS has also been associ...
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| Principais autores: | , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Emergency Department of Hospital San Pedro (Logroño, Spain)
2022-12-01
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| Serija: | Iberoamerican Journal of Medicine |
| Teme: | |
| Online dostop: | https://doi.org/10.53986/ibjm.2023.0006 |
| Oznake: |
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