U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Decreased level of coenzyme Q10 in skeletal muscle

MedGen UID:
764872
Concept ID:
C3551958
Finding
Synonym: Decreased levels of coenzyme Q10 in skeletal muscle
 
HPO: HP:0034369

Definition

Reduced amount of coenzyme Q10,a naturally occurring quinone, in skeletal muscle tissue. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVDecreased level of coenzyme Q10 in skeletal muscle

Conditions with this feature

Autosomal recessive ataxia due to ubiquinone deficiency
MedGen UID:
436985
Concept ID:
C2677589
Disease or Syndrome
Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive multiple-system atrophy-like phenotype (neurodegeneration with autonomic failure and various combinations of parkinsonism and cerebellar ataxia, and pyramidal dysfunction); and dystonia, spasticity, seizures, and intellectual disability. Steroid-resistant nephrotic syndrome (SRNS), the hallmark renal manifestation, is often the initial manifestation either as isolated renal involvement that progresses to end-stage renal disease (ESRD), or associated with encephalopathy (seizures, stroke-like episodes, severe neurologic impairment) resulting in early death. Hypertrophic cardiomyopathy (HCM), retinopathy or optic atrophy, and sensorineural hearing loss can also be seen.
Coenzyme Q10 deficiency, primary, 1
MedGen UID:
764868
Concept ID:
C3551954
Disease or Syndrome
Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive multiple-system atrophy-like phenotype (neurodegeneration with autonomic failure and various combinations of parkinsonism and cerebellar ataxia, and pyramidal dysfunction); and dystonia, spasticity, seizures, and intellectual disability. Steroid-resistant nephrotic syndrome (SRNS), the hallmark renal manifestation, is often the initial manifestation either as isolated renal involvement that progresses to end-stage renal disease (ESRD), or associated with encephalopathy (seizures, stroke-like episodes, severe neurologic impairment) resulting in early death. Hypertrophic cardiomyopathy (HCM), retinopathy or optic atrophy, and sensorineural hearing loss can also be seen.
Coenzyme Q10 deficiency, primary, 3
MedGen UID:
766272
Concept ID:
C3553358
Disease or Syndrome
Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive multiple-system atrophy-like phenotype (neurodegeneration with autonomic failure and various combinations of parkinsonism and cerebellar ataxia, and pyramidal dysfunction); and dystonia, spasticity, seizures, and intellectual disability. Steroid-resistant nephrotic syndrome (SRNS), the hallmark renal manifestation, is often the initial manifestation either as isolated renal involvement that progresses to end-stage renal disease (ESRD), or associated with encephalopathy (seizures, stroke-like episodes, severe neurologic impairment) resulting in early death. Hypertrophic cardiomyopathy (HCM), retinopathy or optic atrophy, and sensorineural hearing loss can also be seen.
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome
MedGen UID:
766288
Concept ID:
C3553374
Disease or Syndrome
Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive multiple-system atrophy-like phenotype (neurodegeneration with autonomic failure and various combinations of parkinsonism and cerebellar ataxia, and pyramidal dysfunction); and dystonia, spasticity, seizures, and intellectual disability. Steroid-resistant nephrotic syndrome (SRNS), the hallmark renal manifestation, is often the initial manifestation either as isolated renal involvement that progresses to end-stage renal disease (ESRD), or associated with encephalopathy (seizures, stroke-like episodes, severe neurologic impairment) resulting in early death. Hypertrophic cardiomyopathy (HCM), retinopathy or optic atrophy, and sensorineural hearing loss can also be seen.
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
MedGen UID:
1799985
Concept ID:
C5568562
Disease or Syndrome
Primary coenzyme Q10 (CoQ10) deficiency is usually associated with multisystem involvement, including neurologic manifestations such as fatal neonatal encephalopathy with hypotonia; a late-onset slowly progressive multiple-system atrophy-like phenotype (neurodegeneration with autonomic failure and various combinations of parkinsonism and cerebellar ataxia, and pyramidal dysfunction); and dystonia, spasticity, seizures, and intellectual disability. Steroid-resistant nephrotic syndrome (SRNS), the hallmark renal manifestation, is often the initial manifestation either as isolated renal involvement that progresses to end-stage renal disease (ESRD), or associated with encephalopathy (seizures, stroke-like episodes, severe neurologic impairment) resulting in early death. Hypertrophic cardiomyopathy (HCM), retinopathy or optic atrophy, and sensorineural hearing loss can also be seen.

Professional guidelines

PubMed

Silva HNMD, Fernandes EM, Pereira VA, Mizobuti DS, Covatti C, Rocha GLD, Minatel E
PLoS One 2024;19(3):e0300006. Epub 2024 Mar 18 doi: 10.1371/journal.pone.0300006. PMID: 38498472Free PMC Article

Recent clinical studies

Etiology

Liu XY, Chen XJ, Zhao M, Wang ZQ, Chen HZ, Li HF, Wang CJ, Wu SF, Peng C, Yin Y, Fu HX, Lin MT, Yu L, Xiong ZQ, Wu ZY, Wang N
J Inherit Metab Dis 2021 Mar;44(2):450-468. Epub 2021 Jan 25 doi: 10.1002/jimd.12361. PMID: 33438237
Dohlmann TL, Morville T, Kuhlman AB, Chrøis KM, Helge JW, Dela F, Larsen S
J Clin Endocrinol Metab 2019 Jul 1;104(7):2501-2508. doi: 10.1210/jc.2018-01185. PMID: 30299473
Ahmadi Y, Ghorbanihaghjo A, Naghi-Zadeh M, Yagin NL
Inflammopharmacology 2018 Jun;26(3):667-674. Epub 2018 Mar 24 doi: 10.1007/s10787-018-0469-x. PMID: 29574631
Gvozdjakova A, Kucharska J, Sykora L, Singh RB
Front Biosci (Schol Ed) 2014 Jan 1;6(1):29-38. doi: 10.2741/s411. PMID: 24389258
Littarru GP, Langsjoen P
Mitochondrion 2007 Jun;7 Suppl:S168-74. Epub 2007 Mar 27 doi: 10.1016/j.mito.2007.03.002. PMID: 17482884

Diagnosis

Hernández-Camacho JD, Vicente-García C, Ardila-García L, Padilla-Campos A, López-Lluch G, Santos-Ocaña C, Zammit PS, Carvajal JJ, Navas P, Fernández-Ayala DJM
J Cachexia Sarcopenia Muscle 2024 Dec;15(6):2402-2416. Epub 2024 Oct 2 doi: 10.1002/jcsm.13574. PMID: 39354863Free PMC Article
Diaz-Vegas A, Madsen S, Cooke KC, Carroll L, Khor JXY, Turner N, Lim XY, Astore MA, Morris JC, Don AS, Garfield A, Zarini S, Zemski Berry KA, Ryan AP, Bergman BC, Brozinick JT, James DE, Burchfield JG
Elife 2023 Dec 27;12 doi: 10.7554/eLife.87340. PMID: 38149844Free PMC Article
Ahmadi Y, Ghorbanihaghjo A, Naghi-Zadeh M, Yagin NL
Inflammopharmacology 2018 Jun;26(3):667-674. Epub 2018 Mar 24 doi: 10.1007/s10787-018-0469-x. PMID: 29574631
Su XW, Nandar W, Neely EB, Simmons Z, Connor JR
Muscle Nerve 2016 Aug;54(2):284-91. Epub 2016 May 19 doi: 10.1002/mus.25048. PMID: 26799243Free PMC Article
Lamperti C, Naini A, Hirano M, De Vivo DC, Bertini E, Servidei S, Valeriani M, Lynch D, Banwell B, Berg M, Dubrovsky T, Chiriboga C, Angelini C, Pegoraro E, DiMauro S
Neurology 2003 Apr 8;60(7):1206-8. doi: 10.1212/01.wnl.0000055089.39373.fc. PMID: 12682339

Therapy

Broome SC, Whitfield J, Karagounis LG, Hawley JA
Sports Med 2024 Sep;54(9):2291-2309. Epub 2024 Jul 26 doi: 10.1007/s40279-024-02072-7. PMID: 39060742Free PMC Article
Kloer HU, Belardinelli R, Ruchong O, Rosenfeldt F
Heart Lung Circ 2020 Feb;29(2):188-195. Epub 2019 Sep 20 doi: 10.1016/j.hlc.2019.08.017. PMID: 31668616
Ahmadi Y, Ghorbanihaghjo A, Naghi-Zadeh M, Yagin NL
Inflammopharmacology 2018 Jun;26(3):667-674. Epub 2018 Mar 24 doi: 10.1007/s10787-018-0469-x. PMID: 29574631
Littarru GP, Langsjoen P
Mitochondrion 2007 Jun;7 Suppl:S168-74. Epub 2007 Mar 27 doi: 10.1016/j.mito.2007.03.002. PMID: 17482884
Cooper JM, Schapira AH
Biofactors 2003;18(1-4):163-71. doi: 10.1002/biof.5520180219. PMID: 14695932

Prognosis

González-Quintana A, García-Consuegra I, Belanger-Quintana A, Serrano-Lorenzo P, Lucia A, Blázquez A, Docampo J, Ugalde C, Morán M, Arenas J, Martín MA
Genes (Basel) 2020 Jul 26;11(8) doi: 10.3390/genes11080855. PMID: 32722639Free PMC Article
Su XW, Nandar W, Neely EB, Simmons Z, Connor JR
Muscle Nerve 2016 Aug;54(2):284-91. Epub 2016 May 19 doi: 10.1002/mus.25048. PMID: 26799243Free PMC Article
Asencio C, Rodríguez-Hernandez MA, Briones P, Montoya J, Cortés A, Emperador S, Gavilán A, Ruiz-Pesini E, Yubero D, Montero R, Pineda M, O'Callaghan MM, Alcázar-Fabra M, Salviati L, Artuch R, Navas P
Eur J Hum Genet 2016 Mar;24(3):367-72. Epub 2015 May 27 doi: 10.1038/ejhg.2015.112. PMID: 26014431Free PMC Article
Littarru GP, Langsjoen P
Mitochondrion 2007 Jun;7 Suppl:S168-74. Epub 2007 Mar 27 doi: 10.1016/j.mito.2007.03.002. PMID: 17482884
Cooper JM, Schapira AH
Biofactors 2003;18(1-4):163-71. doi: 10.1002/biof.5520180219. PMID: 14695932

Clinical prediction guides

González-Quintana A, García-Consuegra I, Belanger-Quintana A, Serrano-Lorenzo P, Lucia A, Blázquez A, Docampo J, Ugalde C, Morán M, Arenas J, Martín MA
Genes (Basel) 2020 Jul 26;11(8) doi: 10.3390/genes11080855. PMID: 32722639Free PMC Article
Ramelli GP, Gallati S, Weis J, Krähenbühl S, Burgunder JM
J Child Neurol 2006 Mar;21(3):253-5. doi: 10.2310/7010.2006.00047. PMID: 16901431
Chu G, Egnaczyk GF, Zhao W, Jo SH, Fan GC, Maggio JE, Xiao RP, Kranias EG
Circ Res 2004 Feb 6;94(2):184-93. Epub 2003 Nov 13 doi: 10.1161/01.RES.0000107198.90218.21. PMID: 14615292
Cooper JM, Schapira AH
Biofactors 2003;18(1-4):163-71. doi: 10.1002/biof.5520180219. PMID: 14695932
Butler MG, Dasouki M, Bittel D, Hunter S, Naini A, DiMauro S
Am J Med Genet A 2003 Jun 1;119A(2):168-71. doi: 10.1002/ajmg.a.10055. PMID: 12749057Free PMC Article

Supplemental Content

Table of contents

    Clinical resources

    Practice guidelines

    • PubMed
      See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.
    • Bookshelf
      See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the FAQ for details.

    Consumer resources

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...