Literature DB >> 25054987

From exercise intolerance to functional improvement: the second wind phenomenon in the identification of McArdle disease.

Renata Siciliani Scalco1, Sherryl Chatfield1, Richard Godfrey1, Jatin Pattni1, Charlotte Ellerton1, Andrea Beggs1, Stefen Brady1, Andrew Wakelin2, Janice L Holton1, Ros Quinlivan1.   

Abstract

McArdle disease is the most common of the glycogen storage diseases. Onset of symptoms is usually in childhood with muscle pain and restricted exercise capacity. Signs and symptoms are often ignored in children or put down to 'growing pains' and thus diagnosis is often delayed. Misdiagnosis is not uncommon because several other conditions such as muscular dystrophy and muscle channelopathies can manifest with similar symptoms. A simple exercise test performed in the clinic can however help to identify patients by revealing the second wind phenomenon which is pathognomonic of the condition. Here a patient is reported illustrating the value of using a simple 12 minute walk test.

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Year:  2014        PMID: 25054987     DOI: 10.1590/0004-282x20140062

Source DB:  PubMed          Journal:  Arq Neuropsiquiatr        ISSN: 0004-282X            Impact factor:   1.420


  6 in total

Review 1.  Can hyperuricemia predict glycogen storage disease (McArdle's disease) in rheumatology practice? (Myogenic hyperuricemia).

Authors:  Döndü Üsküdar Cansu; Bahattin Erdoğan; Cengiz Korkmaz
Journal:  Clin Rheumatol       Date:  2019-05-01       Impact factor: 2.980

2.  McArdle's disease: A differential diagnosis of idiopathic toe walking.

Authors:  David Pomarino; Stephan Martin; Andrea Pomarino; Stefanie Morigeau; Saskia Biskup
Journal:  J Orthop       Date:  2018-05-08

3.  Manifesting heterozygotes in McArdle disease: a myth or a reality-role of statins.

Authors:  Judit Núñez-Manchón; Alfonsina Ballester-Lopez; Emma Koehorst; Ian Linares-Pardo; Daniëlle Coenen; Ignacio Ara; Carlos Rodriguez-Lopez; Alba Ramos-Fransi; Alicia Martínez-Piñeiro; Giuseppe Lucente; Miriam Almendrote; Jaume Coll-Cantí; Guillem Pintos-Morell; Alejandro Santos-Lozano; Joaquin Arenas; Miguel Angel Martín; Mauricio de Castro; Alejandro Lucia; Alfredo Santalla; Gisela Nogales-Gadea
Journal:  J Inherit Metab Dis       Date:  2018-06-20       Impact factor: 4.982

Review 4.  Rhabdomyolysis: a genetic perspective.

Authors:  Renata Siciliani Scalco; Alice R Gardiner; Robert Ds Pitceathly; Edmar Zanoteli; Jefferson Becker; Janice L Holton; Henry Houlden; Heinz Jungbluth; Ros Quinlivan
Journal:  Orphanet J Rare Dis       Date:  2015-05-02       Impact factor: 4.123

5.  McArdle Disease Misdiagnosed as Meningitis.

Authors:  Renata Siciliani Scalco; Sherryl Chatfield; Muhammad Hyder Junejo; Suzanne Booth; Jatin Pattni; Richard Godfrey; Ros Quinlivan
Journal:  Am J Case Rep       Date:  2016-11-30

6.  McArdle disease and pregnancy: A case report and scoping review of pregnancy outcomes.

Authors:  Christopher M Nash; Nabha Shetty; Ashley Miller; Kyle McCoy
Journal:  Obstet Med       Date:  2021-05-27
  6 in total

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