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Volumn 8, Issue 6, 2004, Pages 313-316
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A severe case of facioscapulohumeral muscular dystrophy (FSHD) with some uncommon clinical features and a short 4q35 fragment
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Author keywords
Hyperlordosis; Infantile onset FSHD; Progressive ptosis; Severe
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Indexed keywords
DNA FRAGMENT;
ARTICLE;
BODY POSTURE;
CASE REPORT;
CHROMOSOME 4Q;
CHROMOSOME MOSAICISM;
CLINICAL EXAMINATION;
CLINICAL FEATURE;
DISEASE SEVERITY;
DNA DETERMINATION;
ELECTROMYOGRAPHY;
FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY;
FEMALE;
GENE FREQUENCY;
HUMAN;
LORDOSIS;
ONSET AGE;
PATHOGENESIS;
PRIORITY JOURNAL;
PTOSIS;
SCHOOL CHILD;
SPINE RADIOGRAPHY;
BLEPHAROPTOSIS;
CHILD;
DEOXYRIBONUCLEASE ECORI;
DNA;
ELECTROENCEPHALOGRAPHY;
ELECTROMYOGRAPHY;
FAMILY;
FEMALE;
GENE DELETION;
HUMANS;
LORDOSIS;
MUSCULAR DYSTROPHY, FACIOSCAPULOHUMERAL;
TOMOGRAPHY, X-RAY COMPUTED;
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EID: 8644275568
PISSN: 10903798
EISSN: None
Source Type: Journal
DOI: 10.1016/j.ejpn.2004.08.004 Document Type: Article |
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Times cited : (14)
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References (5)
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