Lissencephaly: Computed tomographic diagnosis |
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| Affiliation: | 1. School of Chemical Technology, Kalinga Institute of Industrial Technology, Bhubaneswar 751024, India;2. Department of Chemical Engineering, Indian Institute of Technology Madras, Chennai, Tamil Nadu 600036, India;3. Department of Earth Resources & Environmental Engineering, Hanyang University, 222-Wangsimni-ro, Seongdong-gu, Seoul 04763, Republic of Korea;4. Chemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia;5. Electronics and Communications Engineering Department, Haldia Institute of Technology, Haldia, India;1. Division of Nephrology, Stanford University School of Medicine, Stanford, CA, United States;2. Division of Endocrinology, Gerontology, and Metabolism, Stanford University School of Medicine, Stanford, CA, United States;3. Stanford Diabetes Research Center, Stanford University School of Medicine, Stanford, CA, United States;4. Division of Primary Care and Population health, Stanford University School of Medicine, Stanford, CA, United States;5. Stanford Prevention Research Center, Stanford University School of Medicine, Stanford, CA, United States;6. Section of Nephrology, Department of Medicine, Baylor College of Medicine, Houston, TX, United States |
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| Abstract: | Lissencephaly is a rare congenital condition with distinctive brain changes. Most of these changes were demonstrated on computed tomography, and include lack of cortical sulci and gyri; calcification in the region of paraphysis; wide, shallow sylvian fissures; colpocephaly; poor development of white matter; and persistent cavum septum pellucidum and cavum vergae. |
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