The differential diagnosis of children with joint hypermobility: A review of the literature

Pediatric Rheumatology

Volumn 7, Issue , 2009, Pages

  Tofts, Louise J ^a,b   Elliott, Elizabeth J ^a,b   Munns, Craig ^a,b   Pacey, Verity ^a,b   Sillence, David O ^a,b  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b UNIVERSITY OF SYDNEY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; COLLAGEN TYPE 3; COLLAGEN TYPE 5; FIBRILLIN 1; TRANSFORMING GROWTH FACTOR BETA RECEPTOR 1;

BONE TURNOVER; CLINICAL FEATURE; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; DUAL ENERGY X RAY ABSORPTIOMETRY; EHLERS DANLOS SYNDROME; GENE MUTATION; GENETIC ANALYSIS; HUMAN; JOINT HYPERMOBILITY; JOINT INSTABILITY; JOINT LAXITY; LABORATORY DIAGNOSIS; MARFAN SYNDROME; MUSCLE STRENGTH; MUSCLE WEAKNESS; OSTEOGENESIS IMPERFECTA; OSTEOPENIA; PRIORITY JOURNAL; REVIEW; RISK FACTOR; SKIN TEST;

EID: 61349175959     PISSN: None     EISSN: 15460096     Source Type: Journal    
DOI: 10.1186/1546-0096-7-1     Document Type: Review

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