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Attribution 4.0 International (CC BY 4.0)
Summary
Author:Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, Chelban V, Manole A, Hamed SA, Haridy NA, Federoff M, Preza E, Hughes D, Pittman A, Jaunmuktane Z, Brandner S, Xiromerisiou G, Wiethoff S, Schottlaender L, Proukakis C, Morris H, Warner T, Bhatia KP, Korlipara LV, Singleton AB, Hardy J, Wood NW, Lewis PA, Houlden H,1 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, Alzheimer's Disease Research Centre, Department of Neurology, Harvard Medical School and Massachusetts General Hospital (OPeni/National library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4939695_aww111f3p&query=Hereditary%20spastic%20paraplegia&it=xg&req=4&npos=79 Description:aww111-F3: Photographs of the hands of Case 33 with ZFYVE26/SPG15 mutation (homozygous p.R1378* mutation). Showing the adducted thumbs that are similar to those seen in MASA (mental retardation, aphasia, shuffling gait and adducted thumbs) syndrome. Age of patient: 34 years.
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| Date/Time | Thumbnail | Dimensions | User | Comment |
|---|
| current | 18:04, 16 October 2021 |  | 512 × 174 (182 KB) | Ozzie10aaaa | Author:Kara E, Tucci A, Manzoni C, Lynch DS, Elpidorou M, Bettencourt C, Chelban V, Manole A, Hamed SA, Haridy NA, Federoff M, Preza E, Hughes D, Pittman A, Jaunmuktane Z, Brandner S, Xiromerisiou G, Wiethoff S, Schottlaender L, Proukakis C, Morris H, Warner T, Bhatia KP, Korlipara LV, Singleton AB, Hardy J, Wood NW, Lewis PA, Houlden H,1 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, Alzheimer's Disease Research Centre, Department of Neurology, Harvard Medic... |
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