Bilateral frontal polymicrogyria and Ehlers-Danlos syndrome.] |
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| Authors: | H Ezzeddine P Sabouraud C Eschard O El Tourjuman N Bednarek J Motte |
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| Institution: | 1. From the Department of Internal Medicine, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Université Claude Bernard Lyon 1 (C.F.), Lyon;2. Laboratoire UMR-CNRS 5303: Laboratory of Tissue Biology and Therapeutic Engineering, Institute of Biology and Protein Chemistry (C.F., T.E.-J.), Lyon;3. Department of Ophthalmology, Hôpital de la Croix-Rousse, Hospices Civils de Lyon, Université Claude Bernard Lyon 1 (L.K., T.M.), Lyon;4. Laboratoire UMR-CNRS 5510 Matéis, Université Claude Bernard Lyon 1 (L.K.), Villeurbanne;5. Department of Ophthalmology, Hôpital Edouard Herriot, Hospices Civils de Lyon, Université Claude Bernard Lyon 1 (C.B.), Lyon;6. Department of Internal Medicine, Hôpital Edouard Herriot, Hospices Civils de Lyon, Université Claude Bernard Lyon 1 (A.H.), Lyon;7. Department of Internal Medicine, Centre Hospitalier Saint-Joseph Saint-Luc, Université Claude Bernard, Lyon 1 (L.P.), Lyon;8. Lyon Immunology FEderation (LIFE) (C.F., Y.J.), Lyon;9. University Claude Bernard Lyon 1, Research on Healthcare Performance (RESHAPE), INSERM U1290 (C.F., P.S.), Lyon, France |
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| Abstract: | The authors describe the case of a six-year-old girl with Ehlers-Danlos syndrome associated to bilateral symmetrical frontal polymicrogyria. Several extracellular matrix components, including collagen, are directly implicated in the neuronal migration. We think that a defect in collagen or in another extracellular matrix protein during fetal development could result in this association. |
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