DMD is the most common muscular dystrophy. The incidence of DMD is estimated at around 1 in 5000 live male births.[8]Ellis JA, Vroom E, Muntoni F. 195th ENMC International Workshop: newborn screening for Duchenne muscular dystrophy 14-16th December, 2012, Naarden, The Netherlands. Neuromuscul Disord. 2013 Aug;23(8):682-9.
https://www.nmd-journal.com/article/S0960-8966(13)00152-1/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/23791627?tool=bestpractice.com
[9]Ryder S, Leadley RM, Armstrong N, et al. The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review. Orphanet J Rare Dis. 2017 Apr 26;12(1):79.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-017-0631-3
http://www.ncbi.nlm.nih.gov/pubmed/28446219?tool=bestpractice.com
[10]Birnkrant DJ, Bushby K, Bann CM, et al; DMD Care Considerations Working Group. Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management. Lancet Neurol. 2018 Mar;17(3):251-67.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869704
http://www.ncbi.nlm.nih.gov/pubmed/29395989?tool=bestpractice.com
One study reported a point prevalence of 1.9 per 100,000 males in the US, with values for the UK, Canada, and France of 2.2, 6.1, and 10.9 per 100,000 males, respectively.[9]Ryder S, Leadley RM, Armstrong N, et al. The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review. Orphanet J Rare Dis. 2017 Apr 26;12(1):79.
https://ojrd.biomedcentral.com/articles/10.1186/s13023-017-0631-3
http://www.ncbi.nlm.nih.gov/pubmed/28446219?tool=bestpractice.com
Incidence has been reported to be decreasing in industrialized countries due to medical advances and reproductive planning.[8]Ellis JA, Vroom E, Muntoni F. 195th ENMC International Workshop: newborn screening for Duchenne muscular dystrophy 14-16th December, 2012, Naarden, The Netherlands. Neuromuscul Disord. 2013 Aug;23(8):682-9.
https://www.nmd-journal.com/article/S0960-8966(13)00152-1/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/23791627?tool=bestpractice.com
The related condition Becker muscular dystrophy (BMD) has a reported prevalence of less than 8 per 100,000 males.[11]Duan D, Goemans N, Takeda S, et al. Duchenne muscular dystrophy. Nat Rev Dis Primers. 2021 Feb 18;7(1):13.
https://www.nature.com/articles/s41572-021-00248-3
http://www.ncbi.nlm.nih.gov/pubmed/33602943?tool=bestpractice.com
Girls or women with DMD or BMD are very rare; some female carriers of the affected gene may show mild symptoms.[11]Duan D, Goemans N, Takeda S, et al. Duchenne muscular dystrophy. Nat Rev Dis Primers. 2021 Feb 18;7(1):13.
https://www.nature.com/articles/s41572-021-00248-3
http://www.ncbi.nlm.nih.gov/pubmed/33602943?tool=bestpractice.com
Other less common muscular dystrophies include myotonic dystrophy, an autosomal dominant disorder that has a reported prevalence of between 1 in 3000 and 1 in 8000 people.[12]Ashizawa T, Gagnon C, Groh WJ, et al. Consensus-based care recommendations for adults with myotonic dystrophy type 1. Neurol Clin Pract. 2018 Dec;8(6):507-20.
https://cp.neurology.org/content/8/6/507
http://www.ncbi.nlm.nih.gov/pubmed/30588381?tool=bestpractice.com
Facioscapulohumeral muscular dystrophy has a reported prevalence of between 1 in 15,000 and 1 in 20,000 people.[13]Tawil R, Kissel JT, Heatwole C, et al. Evidence-based guideline summary: evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy: report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. Neurology. 2015 Jul 28;85(4):357-64.
https://n.neurology.org/content/85/4/357
http://www.ncbi.nlm.nih.gov/pubmed/26215877?tool=bestpractice.com
Limb-girdle muscular dystrophies are rare, with an estimated combined minimum prevalence of 2.38 per 100,000 people, and may have autosomal dominant, autosomal recessive, or sporadic inheritance.[14]Narayanaswami P, Weiss M, Selcen D, et al. Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the guideline development subcommittee of the American Academy of Neurology and the practice issues review panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. Neurology. 2014 Oct 14;83(16):1453-63.
https://n.neurology.org/content/83/16/1453
http://www.ncbi.nlm.nih.gov/pubmed/25313375?tool=bestpractice.com
Congenital muscular dystrophies, a heterogeneous group of rare muscular dystrophies that usually have autosomal recessive transmission, have an estimated prevalence of around 1 in 100,000 people in European populations.[15]Kang PB, Morrison L, Iannaccone ST, et al. Evidence-based guideline summary: evaluation, diagnosis, and management of congenital muscular dystrophy: report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular & Electrodiagnostic Medicine. Neurology. 2015 Mar 31;84(13):1369-78.
https://n.neurology.org/content/84/13/1369
http://www.ncbi.nlm.nih.gov/pubmed/25825463?tool=bestpractice.com
Spinal muscular atrophy (SMA) has an estimated incidence of approximately 1 in 11,000 live births. There is evidence of improved survival and outcomes in recent years.[3]Mercuri E, Finkel RS, Muntoni F, et al; SMA Care Group. Diagnosis and management of spinal muscular atrophy: part 1: recommendations for diagnosis, rehabilitation, orthopedic and nutritional care. Neuromuscul Disord. 2018 Feb;28(2):103-15.
https://www.nmd-journal.com/article/S0960-8966(17)31284-1/fulltext
http://www.ncbi.nlm.nih.gov/pubmed/29290580?tool=bestpractice.com
SMA is an autosomal recessive disease; approximately 2% of cases are due to a new gene mutation.[16]American College of Obstetricians and Gynecologists Committee on Genetics. Committee Opinion No. 691: carrier screening for genetic conditions. Obstet Gynecol. 2017 Mar;129(3):e41-55.
http://www.ncbi.nlm.nih.gov/pubmed/28225426?tool=bestpractice.com