Temporal and spatial gait characteristics of children with Hurler syndrome after umbilical cord blood transplantation

Physical Therapy

Volumn 87, Issue 8, 2007, Pages 978-985

  Dusing, Stacey C ^a   Thorpe, Deborah E ^b   Mercer, Vicki S ^c   Rosenberg, Angela E ^c   Poe, Michele D ^d   Escolar, Maria L ^c  

^a VIRGINIA COMMONWEALTH UNIVERSITY   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF NORTH CAROLINA   (United States)

^d UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BODY BUILD; CHILD DEVELOPMENT; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FUNCTIONAL ASSESSMENT; GAIT; HUMAN; HURLER SYNDROME; MALE; OUTCOME ASSESSMENT; PARAMETER; PRESCHOOL CHILD; SCHOOL CHILD; TRANSPLANTATION; UMBILICAL CORD BLOOD; VELOCITY;

CHILD; CHILD, PRESCHOOL; CORD BLOOD STEM CELL TRANSPLANTATION; FEMALE; GAIT; HUMANS; INFANT; LINEAR MODELS; MALE; MUCOPOLYSACCHARIDOSIS I;

EID: 34547633304     PISSN: 00319023     EISSN: None     Source Type: Journal    
DOI: 10.2522/ptj.20060196     Document Type: Article

References (25)

1. Poorthuis BJ, Wevers RA, Kleijer WJ, et al. The frequency of lysosomal storage diseases in the Netherlands. Hum Genet. 1999;105:151-156.
2. Neufeld EF. Muenzer J. The mucopolysaccharidoses. In: Scriver CR, Beaudet AM, Sly WS, Valle D, eds. The Metabolic and Molecular Basis of Inherited Disease. Vol 3. 8th ed. New York, NY: McGraw-Hill; 2001:3421-3452.
3. Muenzer J. Mucopolysaccharidoses. Adv Pediatr. 1986;33:269-302.
4. Dusing SC, Thorpe DE, Rosenberg AE, et al. Gross motor abilities in children with Hurler syndrome: a case series. Dev Med Child Neurol. 2006;48:927-930.
5. Shull RM, Kakkis ED, McEntee MF, et al. Enzyme replacement in a canine model of Hurler syndrome. Proc Natl Acad Sci U S A. 1994;91:12937-12941.
6. Peters C, Shapiro EG, Anderson J, et al, for the Storage Disease Collaborative Study Group. Hurler syndrome, II: outcome of HLA-genotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. Blood. 1998;91:2601-2608.
7. Weisstein JS, Delgado E, Steinbach LS, et al. Musculoskeletal manifestations of Hurler syndrome: long-term follow-up after bone marrow transplantation. J Pediatr Orthop. 2004;24:97-101.
8. Staba SL, Escolar ML, Poe MD, et al. Cordblood transplants from unrelated donors in patients with Hurler's syndrome. N Engl J Med. 2004;350:1960-1969.
9. Cox-Brinkman J, Boelens JJ, Wraith JE, et al. Haematopoietic cell transplantation (HCT) in combination with enzyme replacement therapy (ERT) in patients with Hurler syndrome. Bone Marrow Transplant. 2006;38:17-21.
10. Bjoraker KJ, Delaney K, Peters C, et al. Long-term outcomes of adaptive functions for children with mucopolysaccharidosis I (Hurler syndrome) treated with hematopoietic stem cell transplantation. J Dev Behav Pediatr. 2006;27:290-296.
11. Hugh-Jones K. Psychomotor development of children with mucopolysaccharidosis type 1-H following bone marrow transplantation. Birth Defects Orig Artic Ser. 1986;22:25-29.
12. Lancioni GE, O'Reilly MF. A review of research on physical exercise with people with severe and profound developmental disabilities. Res Dev Disabil. 1998;19: 477-492.
13. Dykens EM, Rosner BA, Butterbaugh G. Exercise and sports in children and adolescents with developmental disabilities: positive physical and psychosocial effects. Child Adolesc Psychiatr Clin N Am. 1998;7:757-771.
14. Lepage C, Noreau L, Bernard PM. Association between characteristics of locomotion and accomplishment of life habits in children with cerebral palsy. Phys Ther. 1998;78:458-469.
15. Burdette HL, Whitaker RC. Resurrecting free play in young children: looking beyond fitness and fatness to attention, affiliation, and affect. Arch Pediatr Adolesc Med. 2005;159:46-50.
16. Haley SM, Fragala Pinkham MA, Dumas HM, et al. A physical performance measure for individuals with mucopolysaccharidosis type I. Dev Med Child Neurol. 2006;48:576-581.
17. Dumas HM, Fragala MA, Haley SM, et al. Physical performance testing in mucopolysaccharidosis, I: a pilot study. Pediatr Rehabil. 2004;7:125-131.
18. Dusing SC, Thorpe DE. A normative sample of temporal and spatial gait parameters in children and adults using the GAITRite electronic walkway. Gait Posture. 2007; 25:135-139.
19. Thorpe DE, Dusing SC, Moore CG. Repeatability of temporospatial gait measures in children using the GAITRite electronic walkway. Arch Phys Med Rehabil. 2005;86:2342-2346.
20. Hof A. Scaling gait data to body size. Gait Posture. 1996;4:222-223.
21. Stansfield BW, Hillman SJ, Hazlewood ME, et al. Normalisation of gait data in children. Gait Posture. 2003;17:81-87.
22. Singer J, Willett J. Applied longitudinal Data Analysis: Modeling Change and Event Occurrence. New York, NY: Oxford University Press; 2003.
23. Rine RM, Lindeblad S, Donovan P, et al. Balance and motor skills in young children with sensorineural hearing impairment: a preliminary study. Pediatric Physical Therapy. 1996;8(2):55-61.
24. Blomsterwall E, Bilting M, Stephensen H, Wikkelso C. Gait abnormality is not the only motor disturbance in normal pressure hydrocephalus. Scand J Rehabil Med. 1995;27:205-209.
25. Cowan JA, McGirt MJ, Woodworth G, et al. The syndrome of hydrocephalus in young and middle-aged adults (SHYMA). Neurol Res. 2005;27:540-547.