Recurrent central nervous system white matter changes in charcot-Marie-Tooth type X disease

Muscle and Nerve

Volumn 49, Issue 3, 2014, Pages 451-454

  Mckinney, Jennifer L ^a,b   De Los Reyes, Emily C ^a,b   Lo, Warren D ^a,b   Flanigan, Kevin M ^a,b  

^a NATIONWIDE CHILDREN S HOSPITAL   (United States)

^b OHIO STATE UNIVERSITY   (United States)

Author keywords

Connexin 32; GJB1 gene; Hereditary motor and sensory polyneuropathy; Marie; MRI; Tooth disease; X linked Charcot

Indexed keywords

AMOXICILLIN; GAP JUNCTION PROTEIN; GAP JUNCTION PROTEIN 1 PROTEIN; PREDNISONE; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; AUTOIMMUNE DISEASE; BRAIN ELECTROPHYSIOLOGY; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CHILD; CLINICAL EXAMINATION; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; GENE MUTATION; GENETIC ANALYSIS; GUILLAIN BARRE SYNDROME; HEMIPARESIS; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOLECULAR GENETICS; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PERIPHERAL NEUROPATHY; POLYNEUROPATHY; PRIORITY JOURNAL; RECURRENT DISEASE; SCHOOL CHILD; SENSORIMOTOR NEUROPATHY; STREPTOCOCCAL PHARYNGITIS; VASCULITIS; WHITE MATTER LESION; X CHROMOSOME; X LINKED CHARCOT MARIE TOOTH DISEASE;

CONNEXIN 32; GJB1 GENE; HEREDITARY MOTOR AND SENSORY POLYNEUROPATHY; MARIE; MRI; TOOTH DISEASE; X-LINKED CHARCOT;

CENTRAL NERVOUS SYSTEM; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CONNEXINS; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MUTATION; NERVE FIBERS, MYELINATED; NEURAL CONDUCTION; PERIPHERAL NERVES;

EID: 84893920062     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.24108     Document Type: Article

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