Isolated facial diplegia and very late-onset myopathy in two siblings: Atypical presentations of facioscapulohumeral dystrophy

Journal of Neurology

Volumn 257, Issue 3, 2010, Pages 444-446

  Figueroa, Juan J ^a   Chapin, John E ^a  

^a UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

Author keywords

Facial diplegia; Facial weakness; Facioscapulohumeral dystrophy; Limb girdle muscular dystrophy; Myopathy

Indexed keywords

CREATINE KINASE;

ADULT; AGED; ALLELE; ARTICLE; CASE REPORT; CHROMOSOME 4Q; CREATINE KINASE BLOOD LEVEL; DNA HYBRIDIZATION; DNA PROBE; EVOKED MUSCLE RESPONSE; EYE PAIN; FACIAL EXPRESSION; FACIAL NERVE PARALYSIS; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FEMALE; GAIT DISORDER; GENE DELETION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; LIMB WEAKNESS; LORDOSIS; MALE; MUSCLE ATROPHY; MUSCLE EXAMINATION; MUSCLE WEAKNESS; MUTATIONAL ANALYSIS; MYOPATHY; ONSET AGE; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; RESTRICTION FRAGMENT; RESTRICTION MAPPING; SOUTHERN BLOTTING; SYMPTOMATOLOGY;

AGE FACTORS; AGE OF ONSET; AGED; CHROMOSOMES, HUMAN, PAIR 4; DISABILITY EVALUATION; DISEASE PROGRESSION; DNA MUTATIONAL ANALYSIS; FACIAL MUSCLES; FEMALE; GENE DELETION; HUMANS; MALE; MIDDLE AGED; MUSCULAR DISEASES; MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL; MUTATION; PHENOTYPE; SEVERITY OF ILLNESS INDEX;

EID: 77951206247     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-009-5346-5     Document Type: Article

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