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A genetic component in Chiari I malformation: Chiari 1 malformation in all five family members

Under certain classifications, a Chiari type I (CMI) malformation can be characterized as a herniation of the cerebellar tonsils greater than 3 mm. Patients with CMI often have a smaller posterior fossa volume, which results in a smaller amount of space for the cerebellum, leading to the herniation...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Taha F. Hassan, BS, Ryan D. Morgan, BS, Kirie M. Psaromatis, MBA, Benedicto C. Baronia, MD
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Elsevier 2024-04-01
Cyfres:Radiology Case Reports
Pynciau:
Mynediad Ar-lein:http://www.sciencedirect.com/science/article/pii/S1930043323009718
Tagiau: Ychwanegu Tag
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