Literature DB >> 16565891

Camptocormia as a clinical manifestation of mitochondrial myopathy.

José A Gómez-Puerta1, Pilar Peris, Josep M Grau, M Angeles Martinez, Núria Guañabens.   

Abstract

Camptocormia is an unusual condition characterized by a progressive weakness of the extensor muscles of the spine that cause an involuntary truncal flexion. Occasionally, camptocormia can be the clinical manifestation of an underlying myopathy, including inflammatory or metabolic myopathies. We present a case of a 78-year-old female with camptocormia associated with a mitochondrial myopathy. Additionally, we review the clinical characteristics of three similar, previously reported cases.

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Year:  2006        PMID: 16565891     DOI: 10.1007/s10067-006-0259-5

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  11 in total

1.  The old and the new camptocormia.

Authors:  K Karbowski
Journal:  Spine (Phila Pa 1976)       Date:  1999-07-15       Impact factor: 3.468

2.  Camptocormia treated with bilateral pallidal stimulation.

Authors:  Dipankar Nandi; Simon Parkin; Richard Scott; Jonathan L Winter; Carole Joint; Ralph Gregory; John Stein; Tipu Z Aziz
Journal:  J Neurosurg       Date:  2002-08       Impact factor: 5.115

Review 3.  Head drop and camptocormia.

Authors:  T Umapathi; V Chaudhry; D Cornblath; D Drachman; J Griffin; R Kuncl
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-07       Impact factor: 10.154

4.  A note on bent spines: 'camptocormia' and 'head ptosis'.

Authors:  J M S Pearce
Journal:  Eur Neurol       Date:  2005-04-26       Impact factor: 1.710

5.  Camptocormia or cormoptosis? The etymology of the word.

Authors:  D Karras; J Vassilakos; D Kassimos
Journal:  Ann Rheum Dis       Date:  1996-11       Impact factor: 19.103

6.  Camptocormia: pathogenesis, classification, and response to therapy.

Authors:  Shaheda N Azher; Joseph Jankovic
Journal:  Neurology       Date:  2005-08-09       Impact factor: 9.910

7.  Aging and muscle mitochondrial abnormalities.

Authors:  J M Grau; J Casademont; F Cardellach; J Fernàndez-Solà
Journal:  Ann Neurol       Date:  1995-08       Impact factor: 10.422

8.  [Camptocormia: a sign of axial myopathy. Report of 7 cases].

Authors:  V Delcey; E Hachulla; U Michon-Pasturel; V Queyrel; P Y Hatron; N Boutry; V Lemaitre; P Vanhille; J Serratrice; P Disdier; V Juhan; B Devulder; A Thévenon
Journal:  Rev Med Interne       Date:  2002-02       Impact factor: 0.728

9.  [Camptocormia in the elderly patient: myopathy or muscular dystonia?].

Authors:  P Poullin; V Daumen-Legre; G Serratrice
Journal:  Rev Rhum Ed Fr       Date:  1993-02

10.  Is camptocormia a primary muscular disease?

Authors:  M Laroche; M B Delisle; R Aziza; J Lagarrigue; B Mazieres
Journal:  Spine (Phila Pa 1976)       Date:  1995-05-01       Impact factor: 3.468

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  13 in total

Review 1.  Camptocormia in Parkinson's disease: definition, epidemiology, pathogenesis and treatment modalities.

Authors:  Prachaya Srivanitchapoom; Mark Hallett
Journal:  J Neurol Neurosurg Psychiatry       Date:  2015-04-20       Impact factor: 10.154

2.  Camptocormia as a clinical manifestation of polymyositis/systemic sclerosis overlap myositis associated with anti-Ku.

Authors:  Thierry Zenone; Nathalie Streichenberger; Marie Puget
Journal:  Rheumatol Int       Date:  2012-03-28       Impact factor: 2.631

3.  Deep brain stimulation for camptocormia in dystonia and Parkinson's disease.

Authors:  Hans-Holger Capelle; Christoph Schrader; Christian Blahak; Wolfgang Fogel; Thomas M Kinfe; Hansjoerg Baezner; Joachim K Krauss
Journal:  J Neurol       Date:  2010-08-28       Impact factor: 4.849

4.  Painful camptocormia: the relevance of shaking your patient's hand.

Authors:  Arnaud Dupeyron; Nina Stober; Anthony Gelis; Giovani Castelnovo; Pierre Labauge; Jacques Pélissier
Journal:  Eur Spine J       Date:  2009-07-10       Impact factor: 3.134

5.  Pisa syndrome in Parkinson's disease: an electrophysiological and imaging study.

Authors:  Michele Tinazzi; Ina Juergenson; Giovanna Squintani; Gaetano Vattemi; Stefania Montemezzi; Daniela Censi; Paolo Barone; Tommaso Bovi; Alfonso Fasano
Journal:  J Neurol       Date:  2013-05-22       Impact factor: 4.849

6.  Polymyositis-like syndrome caused by hypothyroidism, presenting as camptocormia.

Authors:  Ji Min Kim; Eun Joo Song; Jae Seok Seo; Eon Jeong Nam; Young Mo Kang
Journal:  Rheumatol Int       Date:  2008-08-19       Impact factor: 2.631

7.  A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy.

Authors:  Yusuke Sakiyama; Yuji Okamoto; Itsuro Higuchi; Yukie Inamori; Yoko Sangatsuda; Kumiko Michizono; Osamu Watanabe; Hideyuki Hatakeyama; Yu-ichi Goto; Kimiyoshi Arimura; Hiroshi Takashima
Journal:  Acta Neuropathol       Date:  2011-03-22       Impact factor: 17.088

Review 8.  Camptocormia: Etiology, diagnosis, and treatment response.

Authors:  Farwa Ali; Joseph Y Matsumoto; Anhar Hassan
Journal:  Neurol Clin Pract       Date:  2018-06

9.  Axial mitochondrial myopathy in a patient with rapidly progressive adult-onset scoliosis.

Authors:  Annie Hiniker; Lee-Jun Wong; Sigurd Berven; Cavatina K Truong; Adekunle M Adesina; Marta Margeta
Journal:  Acta Neuropathol Commun       Date:  2014-09-16       Impact factor: 7.801

Review 10.  Pathophysiological Concepts and Treatment of Camptocormia.

Authors:  N G Margraf; A Wrede; G Deuschl; W J Schulz-Schaeffer
Journal:  J Parkinsons Dis       Date:  2016-06-16       Impact factor: 5.568

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