Publications by authors named "Collin Douglas Bray"

Whereas isolated sphenoid wing dysplasia (SWD) is a well-known clinical feature in neurofibromatosis 1 (NF1), extensive cranial defects involving multiple bones have been rarely reported in this disorder. In this report, we describe the clinical course of a 20-year-old male with NF1 and an extensive cranial bone dysplasia. The large sphenoethmoidal defect was associated with transethmoidal and orbital cephalocele as well as inferolateral herniation of the frontal lobe.

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Synopsis of recent research by authors named "Collin Douglas Bray"

  • - Collin Douglas Bray's research primarily explores neuroimaging findings related to cranial bone dysplasia in neurofibromatosis type 1 (NF1), particularly focusing on cases that deviate from typical presentations.
  • - His 2018 article presents a detailed case of a 20-year-old male with NF1 exhibiting extensive sphenoethmoidal dysplasia, a rarity compared to the more common isolated sphenoid wing dysplasia.
  • - The study elucidates the clinical implications of the extensive cranial defects, including associated complications such as cephalocele and herniation of the frontal lobe, thereby contributing to the understanding of NF1-related cranial anomalies.