Pierre Robin sequence with a novel mutation in SOX9 gene: Case study

• Main Authors: Mohd Murtaza (Author), Md Niamat Ali (Author), Mahrukh Hameed Zargar (Author)
• פורמט: ספר
• יצא לאור: Elsevier, 2021-06-01T00:00:00Z.
• נושאים: article
• גישה מקוונת: Connect to this object online.

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...