{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,3]],"date-time":"2025-10-03T09:08:10Z","timestamp":1759482490011},"reference-count":20,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,1,1]]},"DOI":"10.7759\/cureus.51428","type":"journal-article","created":{"date-parts":[[2024,1,1]],"date-time":"2024-01-01T08:21:25Z","timestamp":1704097285000},"source":"Crossref","is-referenced-by-count":2,"title":["Management of a 25-Year-Old Female Patient With Limb-Girdle Muscular Dystrophy With Physiotherapy: A Case Report"],"prefix":"10.7759","author":[{"given":"Sojwal P","family":"Nandanwar","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Swadha P","family":"Udhoji","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raghumahanti","family":"Raghuveer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1007\/s11910-010-0119-1","article-title":"Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies","volume":"10","author":"Rocha CT","year":"2010","unstructured":"Rocha CT, Hoffman EP. Limb-girdle and congenital muscular dystrophies: current diagnostics, management, and emerging technologies. Curr Neurol Neurosci Rep. 2010, 10:267-76. 10.1007\/s11910-010-0119-1","journal-title":"Curr Neurol Neurosci Rep"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/77.2.169","article-title":"On the classification, natural history and treatment of the myopathies","volume":"77","author":"WA JN","year":"1954","unstructured":"WA JN, NA FJ. On the classification, natural history and treatment of the myopathies. Brain. 1954, 77:169-231. 10.1093\/brain\/77.2.169","journal-title":"Brain"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1212\/NXG.0000000000200084","article-title":"Longitudinal analysis of respiratory function of different types of limb girdle muscular dystrophies reveals independent trajectories","volume":"9","author":"Muni-Lofra R","year":"2023","unstructured":"Muni-Lofra R, Juanola-Mayos E, Schiava M, et al.. Longitudinal analysis of respiratory function of different types of limb girdle muscular dystrophies reveals independent trajectories. Neurol Genet. 2023, 9:e200084. 10.1212\/NXG.0000000000200084","journal-title":"Neurol Genet"},{"key":"ref4","doi-asserted-by":"publisher","DOI":"10.7759\/cureus.21353","article-title":"Calpainopathy (Leyden-Mobius limb-girdle muscular dystrophy type 2A phenotype) and dysferlinopathy (Miyoshi distal myopathy limb-girdle muscular dystrophy type 2B phenotype) of preadolescent onset: case reports of two male Filipinos","volume":"14","author":"Quilacio JM","year":"2022","unstructured":"Quilacio JM, Rosales RL, Ampil ER. Calpainopathy (Leyden-Mobius limb-girdle muscular dystrophy type 2A phenotype) and dysferlinopathy (Miyoshi distal myopathy limb-girdle muscular dystrophy type 2B phenotype) of preadolescent onset: case reports of two male Filipinos. Cureus. 2022, 14:e21353. 10.7759\/cureus.21353","journal-title":"Cureus"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.19045\/bspab.2023.120028","article-title":"Overview of muscular dystrophy, it\u2019s types, symptoms, management and possible treatment","volume":"12","author":"Liaqat ST","year":"2023","unstructured":"Liaqat ST, Akram F, Waseem R, et al.. Overview of muscular dystrophy, it\u2019s types, symptoms, management and possible treatment. Pure Appl Biol. 2023, 12:261-73. 10.19045\/bspab.2023.120028","journal-title":"Pure Appl Biol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.1093\/brain\/awp236","article-title":"Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population","volume":"132","author":"Norwood FL","year":"2009","unstructured":"Norwood FL, Harling C, Chinnery PF, Eagle M, Bushby K, Straub V. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population. Brain. 2009, 132:3175-86. 10.1093\/brain\/awp236","journal-title":"Brain"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.1055\/s-0041-1736567","article-title":"Disease progression and mutation pattern in a large cohort of LGMD R1\/LGMD 2A patients from India","volume":"9","author":"Ganaraja VH","year":"2022","unstructured":"Ganaraja VH, Polavarapu K, Bardhan M, et al.. Disease progression and mutation pattern in a large cohort of LGMD R1\/LGMD 2A patients from India. Glob Med Genet. 2022, 9:34-41. 10.1055\/s-0041-1736567","journal-title":"Glob Med Genet"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1016\/j.bbadis.2006.07.002","article-title":"Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)","volume":"1772","author":"Kramerova I","year":"2007","unstructured":"Kramerova I, Beckmann JS, Spencer MJ. Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A). Biochim Biophys Acta. 2007, 1772:128-44. 10.1016\/j.bbadis.2006.07.002","journal-title":"Biochim Biophys Acta"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1002\/ana.20283","article-title":"Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I","volume":"56","author":"Poppe M","year":"2004","unstructured":"Poppe M, Bourke J, Eagle M, et al.. Cardiac and respiratory failure in limb-girdle muscular dystrophy 2I. Ann Neurol. 2004, 56:738-41. 10.1002\/ana.20283","journal-title":"Ann Neurol"},{"key":"ref10","article-title":"Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages","volume":"34","author":"SI G","year":"2015","unstructured":"SI G, SI C, GI S, ZA V, AN C, RI G. Muscle exercise in limb girdle muscular dystrophies: pitfall and advantages. Acta Myol. 2015, 34:3-8.","journal-title":"Acta Myol"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1212\/01.wnl.0000250358.32199.24","article-title":"Endurance training: an effective and safe treatment for patients with LGMD2I","volume":"68","author":"Sveen ML","year":"2007","unstructured":"Sveen ML, Jeppesen TD, Hauerslev S, Krag TO, Vissing J. Endurance training: an effective and safe treatment for patients with LGMD2I. Neurology. 2007, 68:59-61. 10.1212\/01.wnl.0000250358.32199.24","journal-title":"Neurology"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.25107\/2638-4558.1158","article-title":"Physiotherapy in calpainopathy (LGMD2A): a case report","volume":"4","author":"Bajpai A","year":"2020","unstructured":"Bajpai A. Physiotherapy in calpainopathy (LGMD2A): a case report. Clin Case Rep Int. 2020, 4:1-5. 10.25107\/2638-4558.1158","journal-title":"Clin Case Rep Int"},{"key":"ref13","doi-asserted-by":"publisher","DOI":"10.1002\/mus.23491","article-title":"Resistance training in patients with limb-girdle and becker muscular dystrophies","volume":"47","author":"Sveen ML","year":"2013","unstructured":"Sveen ML, Andersen SP, Ingelsrud LH, et al.. Resistance training in patients with limb-girdle and becker muscular dystrophies. Muscle Nerve. 2013, 47:163-9. 10.1002\/mus.23491","journal-title":"Muscle Nerve"},{"key":"ref14","doi-asserted-by":"publisher","DOI":"10.1007\/s12098-022-04444-1","article-title":"Physical therapy-based early intervention in limb-girdle muscular dystrophy","volume":"90","author":"Kunti C","year":"2023","unstructured":"Kunti C, Ryain A, Dogra P, Ghosh A, Parab S. Physical therapy-based early intervention in limb-girdle muscular dystrophy. Indian J Pediatr. 2023, 90:308. 10.1007\/s12098-022-04444-1","journal-title":"Indian J Pediatr"},{"key":"ref15","doi-asserted-by":"publisher","DOI":"10.4103\/0028-3886.241363","article-title":"Commonly available outcome measures for use in Indian boys with Duchenne muscular dystrophy","volume":"66","author":"Arora H","year":"2018","unstructured":"Arora H. Commonly available outcome measures for use in Indian boys with Duchenne muscular dystrophy. Neurol India. 2018, 66:1279-85. 10.4103\/0028-3886.241363","journal-title":"Neurol India"},{"key":"ref16","doi-asserted-by":"publisher","DOI":"10.3390\/cells11040687","article-title":"Outcome measures in facioscapulohumeral muscular dystrophy clinical trials","volume":"11","author":"Ghasemi M","year":"2022","unstructured":"Ghasemi M, Emerson CP Jr, Hayward LJ. Outcome measures in facioscapulohumeral muscular dystrophy clinical trials. Cells. 2022, 11:687. 10.3390\/cells11040687","journal-title":"Cells"},{"key":"ref17","doi-asserted-by":"publisher","DOI":"10.1016\/j.nmd.2022.07.118","article-title":"Rasch analysis of the PROMIS parent proxy item banks administered to\r\ncaregivers of patients with Duchenne muscular dystrophy","volume":"32","author":"Lowes L","year":"2022","unstructured":"Lowes L, Reash N, Alfano L, Iammarino M, LeReun C, Audhya I. Rasch analysis of the PROMIS parent proxy item banks administered to\r\ncaregivers of patients with Duchenne muscular dystrophy. Neuromuscul Disord. 2022, 32:70. 10.1016\/j.nmd.2022.07.118","journal-title":"Neuromuscul Disord"},{"key":"ref18","doi-asserted-by":"publisher","DOI":"10.3390\/pathophysiology28020016","article-title":"Current and future therapeutic strategies for limb girdle muscular dystrophy type r1: clinical and experimental approaches","volume":"28","author":"\u015eahin \u0130O","year":"2021","unstructured":"\u015eahin \u0130O, \u00d6zkul Y, D\u00fcndar M. Current and future therapeutic strategies for limb girdle muscular dystrophy type r1: clinical and experimental approaches. Pathophysiology. 2021, 28:238-49. 10.3390\/pathophysiology28020016","journal-title":"Pathophysiology"},{"key":"ref19","doi-asserted-by":"publisher","DOI":"10.17712\/nsj.2015.3.201501097","article-title":"The effects of electrical stimulation and exercise therapy in patients with limb girdle muscular dystrophy. A controlled clinical trial","volume":"20","author":"Kilin\u00e7 M","year":"2015","unstructured":"Kilin\u00e7 M, Yildirim SA, Tan E. The effects of electrical stimulation and exercise therapy in patients with limb girdle muscular dystrophy. A controlled clinical trial. Neurosciences (Riyadh). 2015, 20:259-66. 10.17712\/nsj.2015.3.201501097","journal-title":"Neurosciences (Riyadh)"},{"key":"ref20","doi-asserted-by":"publisher","DOI":"10.1007\/s00415-023-11837-5","article-title":"Diagnosis and management of Becker muscular dystrophy: the French guidelines","volume":"270","author":"Magot A","year":"2023","unstructured":"Magot A, Wahbi K, Leturcq F, Jaffre S, P\u00e9r\u00e9on Y, Sole G. Diagnosis and management of Becker muscular dystrophy: the French guidelines. J Neurol. 2023, 270:4763-81. 10.1007\/s00415-023-11837-5","journal-title":"J Neurol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/193627-management-of-a-25-year-old-female-patient-with-limb-girdle-muscular-dystrophy-with-physiotherapy-a-case-report","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T20:13:26Z","timestamp":1707509606000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/193627-management-of-a-25-year-old-female-patient-with-limb-girdle-muscular-dystrophy-with-physiotherapy-a-case-report"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,1,1]]},"references-count":20,"URL":"https:\/\/doi.org\/10.7759\/cureus.51428","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,1,1]]}}}