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Scapular muscle hypertrophy

MedGen UID:
868294
•Concept ID:
C4022688
•
Pathologic Function
HPO: HP:0012895

Definition

Muscle hypertrophy affecting the scapular muscles. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVScapular muscle hypertrophy

Professional guidelines

PubMed

Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients.
Unnikrishnan G, Polavarapu K, Bardhan M, Nashi S, Vengalil S, Preethish-Kumar V, Valasani RK, Huddar A, Nishadham V, Nandeesh BN, Nalini A
J Neuromuscul Dis 2023;10(4):615-626. doi: 10.3233/JND-221618. PMID: 37154180Free PMC Article

Recent clinical studies

Etiology

Phenotype Genotype Characterization of FKRP-related Muscular Dystrophy among Indian Patients.
Unnikrishnan G, Polavarapu K, Bardhan M, Nashi S, Vengalil S, Preethish-Kumar V, Valasani RK, Huddar A, Nishadham V, Nandeesh BN, Nalini A
J Neuromuscul Dis 2023;10(4):615-626. doi: 10.3233/JND-221618. PMID: 37154180Free PMC Article
Limb-girdle muscular dystrophy type 2A in Brazilian children.
Albuquerque MA, Abath Neto O, Silva FM, Zanoteli E, Reed UC
Arq Neuropsiquiatr 2015 Dec;73(12):993-7. doi: 10.1590/0004-282X20150168. PMID: 26677118
Hypertrophic changes of the teres minor muscle in rotator cuff tears: quantitative evaluation by magnetic resonance imaging.
Kikukawa K, Ide J, Kikuchi K, Morita M, Mizuta H, Ogata H
J Shoulder Elbow Surg 2014 Dec;23(12):1800-1805. Epub 2014 Jun 4 doi: 10.1016/j.jse.2014.03.014. PMID: 24906902
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.
Bushby K, Anderson LV, Pollitt C, Naom I, Muntoni F, Bindoff L
Brain 1998 Apr;121 ( Pt 4):581-8. doi: 10.1093/brain/121.4.581. PMID: 9577386

Diagnosis

Limb-girdle muscular dystrophy type 2A in Brazilian children.
Albuquerque MA, Abath Neto O, Silva FM, Zanoteli E, Reed UC
Arq Neuropsiquiatr 2015 Dec;73(12):993-7. doi: 10.1590/0004-282X20150168. PMID: 26677118
Clinical reasoning: a 52-year-old woman with progressive proximal weakness.
Enduri S, Taylor MR, Liewluck T
Neurology 2014 Sep 2;83(10):e106-9. doi: 10.1212/WNL.0000000000000757. PMID: 25180003Free PMC Article
The thoracic outlet syndrome in athletes.
Nichols AW
J Am Board Fam Pract 1996 Sep-Oct;9(5):346-55. PMID: 8884673
Suprascapular nerve compression at the spinoglenoid notch.
Kiss G, Kómár J
Muscle Nerve 1990 Jun;13(6):556-7. doi: 10.1002/mus.880130614. PMID: 2366829

Prognosis

Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation.
Merlini L, Kaplan JC, Navarro C, Barois A, Bonneau D, Brasa J, Echenne B, Gallano P, Jarre L, Jeanpierre M, Kalaydjieva L, Leturcq F, Levi-Gomes A, Toutain A, Tournev I, Urtizberea A, Vallat JM, Voit T, Warter JM
Neurology 2000 Mar 14;54(5):1075-9. doi: 10.1212/wnl.54.5.1075. PMID: 10720277

Clinical prediction guides

Upper torso pain and musculoskeletal structure and function in women with and without large breasts: A cross sectional study.
McGhee DE, Coltman KA, Riddiford-Harland DL, Steele JR
Clin Biomech (Bristol, Avon) 2018 Jan;51:99-104. Epub 2017 Dec 21 doi: 10.1016/j.clinbiomech.2017.12.009. PMID: 29287172
Hypertrophic changes of the teres minor muscle in rotator cuff tears: quantitative evaluation by magnetic resonance imaging.
Kikukawa K, Ide J, Kikuchi K, Morita M, Mizuta H, Ogata H
J Shoulder Elbow Surg 2014 Dec;23(12):1800-1805. Epub 2014 Jun 4 doi: 10.1016/j.jse.2014.03.014. PMID: 24906902
Homogeneous phenotype of the gypsy limb-girdle MD with the gamma-sarcoglycan C283Y mutation.
Merlini L, Kaplan JC, Navarro C, Barois A, Bonneau D, Brasa J, Echenne B, Gallano P, Jarre L, Jeanpierre M, Kalaydjieva L, Leturcq F, Levi-Gomes A, Toutain A, Tournev I, Urtizberea A, Vallat JM, Voit T, Warter JM
Neurology 2000 Mar 14;54(5):1075-9. doi: 10.1212/wnl.54.5.1075. PMID: 10720277

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