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...
| Published in: | Iberoamerican Journal of Medicine |
|---|---|
| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
Emergency Department of Hospital San Pedro (Logroño, Spain)
2022-12-01
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| Subjects: | |
| Online Access: | https://doi.org/10.53986/ibjm.2023.0006 |