Tongue atrophy in facioscapulohumeral muscular dystrophy

Neurology

Volumn 57, Issue 4, 2001, Pages 733-735

  Yamanaka, G ^a,b   Goto, K ^a   Matsumura, T ^a   Funakoshi, M ^c   Komori, T ^d   Hayashi, Yukiko K ^a   Arahata, K ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b TOKYO MEDICAL UNIVERSITY   (Japan)

^c JIKEI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d TOKYO METROPOLITAN NEUROLOGICAL HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 4Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; ELECTROMYOGRAPHY; FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY; FEMALE; GENE DELETION; HUMAN; HUMAN CELL; JAPAN; MALE; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PRIORITY JOURNAL; SCHOOL CHILD; TONGUE DISEASE;

EID: 0035964163     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.4.733     Document Type: Article

References (10)

1. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
2. DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: Clinical correlations
3. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: Implications for genetic counselling and etiology of FSHD1
4. Facioscapulohumeral muscular dystrophy
5. Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness
6. Facioscapulohumeral muscular dystrophy in early childhood
7. Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy
8. Genetic counselling in facioscapulohumeral muscular dystrophy
9. Computerized tomography of oropharynx is useful in the diagnosis of OPMD
10. Amyotrophic lateral sclerosis: Abnormalities of the tongue on magnetic resonance imaging