Literature DB >> 19373113

Transient monoparesis after blade plate removal in a Hutchinson-Gilford progeria syndrome patient: a case report.

Suzanne M Yandow1, David L Rimoin, Aimee M Grace, Ramona R Fillman, Ellen M Raney.   

Abstract

Treatment of patients with Hutchinson-Gilford progeria syndrome (HGPS) is based on the abnormalities of accelerated aging that affect the healing processes, combined with a fragile cardiovascular status. A classic HGPS case, of Korean ancestry, previously treated for severe coxa valga with bilateral varus osteotomies using blade plate fixation is presented. Complications over the blade plate area required removal of the hardware, after which the patient showed right-sided hypertonicity--determined to be a cerebrovascular accident. Subsequently, the patient returned almost completely to her presurgical neurologic status. Perioperative planning for HGPS patients should include risks that are typically considered in the planning for geriatric patient care.

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Year:  2009        PMID: 19373113      PMCID: PMC2841562          DOI: 10.1097/BPB.0b013e32832ab928

Source DB:  PubMed          Journal:  J Pediatr Orthop B        ISSN: 1060-152X            Impact factor:   1.041


  6 in total

1.  Report on a case of Hutchinson-Gilford progeria, with special reference to orthopedic problems.

Authors:  F Fernandez-Palazzi; A T McLaren; D F Slowie
Journal:  Eur J Pediatr Surg       Date:  1992-12       Impact factor: 2.191

Review 2.  Hutchinson-Gilford progeria syndrome: review of the phenotype.

Authors:  Raoul C M Hennekam
Journal:  Am J Med Genet A       Date:  2006-12-01       Impact factor: 2.802

3.  Orthopaedic aspects of progeria.

Authors:  C Moen
Journal:  J Bone Joint Surg Am       Date:  1982-04       Impact factor: 5.284

Review 4.  Progeria of stem cells: stem cell exhaustion in Hutchinson-Gilford progeria syndrome.

Authors:  Julius Halaschek-Wiener; Angela Brooks-Wilson
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2007-01       Impact factor: 6.053

5.  Hip disease in Hutchinson-Gilford progeria syndrome.

Authors:  J G Gamble
Journal:  J Pediatr Orthop       Date:  1984-09       Impact factor: 2.324

6.  The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin.

Authors:  Dayle McClintock; Desiree Ratner; Meepa Lokuge; David M Owens; Leslie B Gordon; Francis S Collins; Karima Djabali
Journal:  PLoS One       Date:  2007-12-05       Impact factor: 3.240

  6 in total

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