Literature DB >> 22203329

Pathomechanics of Gowers' sign: a video analysis of a spectrum of Gowers' maneuvers.

Richard F Chang1, Scott J Mubarak.   

Abstract

BACKGROUND: Gowers' sign is a screening test for muscle weakness, typically seen in Duchenne muscular dystrophy but also seen in numerous other conditions. The mildest presentations and the variations of Gowers' sign are poorly described in the literature but are important to recognize to help with early diagnosis of a neuromuscular problem. QUESTIONS/PURPOSES: We therefore (1) defined the characteristics of the mildest forms and the compensatory mechanism used, (2) categorized the spectrum of this sign as seen in various neuromuscular diseases, and (3) provide educational videos for clinicians.
METHODS: We videotaped 33 patients with Gowers' sign and three healthy children. Weakness was categorized as: mild = prolonged or rise using single-hand action; moderate = forming prone crawl position and using one or two hands on thigh; severe = more than two thigh maneuvers, rising with additional aid, or unable to rise.
RESULTS: The earliest changes were exaggerated torso flexion, wide base, and equinus posturing, which reduce hip extension moment, keep forces anterior to the knee, and improve balance. Patients with moderate weakness have wide hip abduction, shifts in pelvic tilt, and lordosis, which reduce knee extension moment, improve hamstrings moment arm, and aide truncal extension. The classic Gowers' sign (severe) exaggerates all mechanisms.
CONCLUSIONS: The classically described Gowers' sign is usually a late finding. However more subtle forms of Gowers' sign including mild hand pressure against the thigh and prone crawl position should be recognized by clinicians to initiate additional diagnostic tests.

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Mesh:

Year:  2011        PMID: 22203329      PMCID: PMC3369091          DOI: 10.1007/s11999-011-2210-6

Source DB:  PubMed          Journal:  Clin Orthop Relat Res        ISSN: 0009-921X            Impact factor:   4.176


  11 in total

1.  Gowers' sign.

Authors:  J M Pearce
Journal:  J Neurol Neurosurg Psychiatry       Date:  2000-02       Impact factor: 10.154

2.  Gower's sign in children with juvenile idiopathic arthritis.

Authors:  E Stathopulu; E Baildam
Journal:  Rheumatology (Oxford)       Date:  2003-08       Impact factor: 7.580

3.  Understanding muscle coordination of the human leg with dynamical simulations.

Authors:  Felix E Zajac
Journal:  J Biomech       Date:  2002-08       Impact factor: 2.712

4.  Atypical presentations of spinal muscular atrophy type III (Kugelberg-Welander disease).

Authors:  P B Kang; K S Krishnamoorthy; R M Jones; F D Shapiro; B T Darras
Journal:  Neuromuscul Disord       Date:  2006-06-22       Impact factor: 4.296

5.  Gowers' sign revisited.

Authors:  G B Wallace; R W Newton
Journal:  Arch Dis Child       Date:  1989-09       Impact factor: 3.791

6.  Classics in neurology. Fragments of neurologic history: pseudohypertrophic muscular dystrophy and Gowers' sign.

Authors:  K L Tyler; L C McHenry
Journal:  Neurology       Date:  1983-01       Impact factor: 9.910

7.  Gowers' sign in children with discitis of the lumbar spine.

Authors:  Yigal Mirovsky; Leonel Copeliovich; Nahum Halperin
Journal:  J Pediatr Orthop B       Date:  2005-03       Impact factor: 1.041

8.  Origins and early descriptions of "Duchenne muscular dystrophy".

Authors:  Kenneth L Tyler
Journal:  Muscle Nerve       Date:  2003-10       Impact factor: 3.217

9.  Functional evaluation of Duchenne muscular dystrophy: proposal for a protocol.

Authors:  F Cornelio; F Dworzak; L Morandi; E Fedrizzi; M R Balestrini; L Gondoni
Journal:  Ital J Neurol Sci       Date:  1982-12

10.  The pathomechanics of gait in Duchenne muscular dystrophy.

Authors:  D H Sutherland; R Olshen; L Cooper; M Wyatt; J Leach; S Mubarak; P Schultz
Journal:  Dev Med Child Neurol       Date:  1981-02       Impact factor: 5.449

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  4 in total

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Authors:  A F Mead; M Petrov; A S Malik; M A Mitchell; M K Childers; J R Bogan; G Seidner; J N Kornegay; H H Stedman
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Review 2.  A Practical Approach to Juvenile Dermatomyositis and Juvenile Scleroderma.

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Journal:  Childs Nerv Syst       Date:  2015-05       Impact factor: 1.475

Review 4.  The skeletal muscle phenotype of children with Neurofibromatosis Type 1 - A clinical perspective.

Authors:  Amish Chinoy; Grace R Vassallo; Emma Burkitt Wright; Judith Eelloo; Siobhan West; Eileen Hupton; Paula Galloway; Amy Pilkington; Raja Padidela; M Zulf Mughal
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  4 in total

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