Pierre Robin sequence with a novel mutation in SOX9 gene: Case study
Background: Pierre Robin Syndrome (PRS) is a rare congenital anomaly characterized by micrognathia, glossoptosis, and cleft palate. The PRS has been found to be associated with the cleft palate with the incidence of 1/8500 to 1/14000 births. Case characteristic: We reported a case of a four-day-old...
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Elsevier,
2021-06-01T00:00:00Z.
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