In this introductory series on neurocutaneous syndromes, Dr. Asim Choudhri focuses on neurofibromatosis type 1 and its numerous manifestations in the pediatric patient population. This course outlines what findings are clinically significant, how to characterize this disease in reports and the best possible steps for disease management and observation.
After completing this course, you will be better able to:
- Apply appropriate search patterns to ensure high quality case assessment
- Identify key anatomical landmarks, variations, and abnormalities on imaging
- Accurately interpret advanced imaging cases
- Formulate definitive diagnoses and limited differentials
Topics :
- Introduction to Neurocutaneous Syndromes
- NF1, Chiari Type 1
- NF1, With Waxing and Waning Cystic Lesion
- Developing myelin vacuolization, Subtle Optic Glioma
- NF1 with Tortuous Optic Nerve
- Bilateral Thalamic vacuolization
- Normal Brain MRI in Patient with Known NF1
- Mild phenotype and Left Sphenoid Wing Dysplasia
- NF1, High grade Glioma
- NF1, Bilateral Optic Glioma
- Focal Optic Pathway Glioma in NF1
- Fusiform Optic Pathway Glioma, NF1
- NF1 with Chasmatic Glioma
- Optic Tract Glioma in NF1 Patient
- NF1, Optic Nerve Glioma, Moya moya
- Developing Right Fusiform Optic Glioma
- Enlarged Right Globe in NF1 patient
- Developing Brainstem Lesion, subtle Optic Glioma
- Buphthalmos, and orbital plexiform neurofibroma
- Sphenoid wing dysplasia on MRI
- Neurocutaneous Syndromes Summary
- NF1, Moya moya
Content reviewed: July 9, 2021
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