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Charcot–Marie–Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family
Mutations in the small heat-shock protein HSP27 gene are associated with distal hereditary motor neuropathy and with the axonal form of Charcot–Marie–Tooth disease type 2. We present the clinical and electrophysiological data on a multigenerational family with the p.Arg136Leu HSP27 mutation. Atypica...
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Published in: | Neurological sciences 2015-06, Vol.36 (6), p.1003-1006 |
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container_title | Neurological sciences |
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creator | Stancanelli, Claudia Fabrizi, Gian Maria Ferrarini, Moreno Cavallaro, Tiziana Taioli, Federica Di Leo, Rita Russo, Massimo Gentile, Luca Toscano, Antonio Vita, Giuseppe Mazzeo, Anna |
description | Mutations in the small heat-shock protein
HSP27
gene are associated with distal hereditary motor neuropathy and with the axonal form of Charcot–Marie–Tooth disease type 2. We present the clinical and electrophysiological data on a multigenerational family with the p.Arg136Leu HSP27 mutation. Atypical features such as deafness and pyramidal signs were present in our cases adding new data to the large spectrum of
HSP27
-related phenotype. |
doi_str_mv | 10.1007/s10072-014-2050-8 |
format | article |
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HSP27
gene are associated with distal hereditary motor neuropathy and with the axonal form of Charcot–Marie–Tooth disease type 2. We present the clinical and electrophysiological data on a multigenerational family with the p.Arg136Leu HSP27 mutation. Atypical features such as deafness and pyramidal signs were present in our cases adding new data to the large spectrum of
HSP27
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HSP27
gene are associated with distal hereditary motor neuropathy and with the axonal form of Charcot–Marie–Tooth disease type 2. We present the clinical and electrophysiological data on a multigenerational family with the p.Arg136Leu HSP27 mutation. Atypical features such as deafness and pyramidal signs were present in our cases adding new data to the large spectrum of
HSP27
-related phenotype.</description><subject>Adult</subject><subject>Aged</subject><subject>Brief Communication</subject><subject>Charcot-Marie-Tooth Disease - genetics</subject><subject>Charcot-Marie-Tooth Disease - physiopathology</subject><subject>Female</subject><subject>HSP27 Heat-Shock Proteins - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Pedigree</subject><subject>Phenotype</subject><subject>Psychiatry</subject><issn>1590-1874</issn><issn>1590-3478</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp1kd1KwzAUx4Mobn48gDcS8Mabar6att7JcCpMFNTrkHanW0fbdEl6sTvfwTf0SczcFBEkkHOS8zv_hPNH6ISSC0pIcunWO4sIFREjMYnSHTSkcUYiLpJ0d5vTNBEDdODcgpBAUr6PBiyORcI5GaLlaK5tYfzH2_uDthWE-GKMn2M2vsLdHFrjV11V4M6Cg9ZrX5kWmxL7OeBrO6NcTqDHd89PLMFNv61XLdbhVPtqBi3Yr0td41I3Vb06Qnulrh0cb-Mheh3fvIzuosnj7f3oehIVQjAf5VMeFtNclwIKEFxCHGeCFUxQzXmSpVnOhEwgL_V0muZZqEvgZS5ZnFGZ8EN0vtHtrFn24LxqKldAXesWTO8UlakM05CMBvTsD7owvQ1f_qJimYZhyUDRDVVY45yFUnW2arRdKUrU2gm18UOFKau1HyoNPadb5T5vYPrT8W1AANgGcKHUzsD-evpf1U_7DJab</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Stancanelli, Claudia</creator><creator>Fabrizi, Gian Maria</creator><creator>Ferrarini, Moreno</creator><creator>Cavallaro, Tiziana</creator><creator>Taioli, Federica</creator><creator>Di Leo, Rita</creator><creator>Russo, Massimo</creator><creator>Gentile, Luca</creator><creator>Toscano, Antonio</creator><creator>Vita, Giuseppe</creator><creator>Mazzeo, Anna</creator><general>Springer Milan</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>K9-</scope><scope>K9.</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20150601</creationdate><title>Charcot–Marie–Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family</title><author>Stancanelli, Claudia ; 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HSP27
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HSP27
-related phenotype.</abstract><cop>Milan</cop><pub>Springer Milan</pub><pmid>25547330</pmid><doi>10.1007/s10072-014-2050-8</doi><tpages>4</tpages></addata></record> |
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subjects | Adult Aged Brief Communication Charcot-Marie-Tooth Disease - genetics Charcot-Marie-Tooth Disease - physiopathology Female HSP27 Heat-Shock Proteins - genetics Humans Male Medicine Medicine & Public Health Middle Aged Mutation Neurology Neuroradiology Neurosciences Neurosurgery Pedigree Phenotype Psychiatry |
title | Charcot–Marie–Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family |
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