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The expanding spectrum of dystrophinopathies: HyperCKemia to manifest female carriers.

Authors :
Suthar, Renu
Kesavan, Shivan
Sharawat, Indar
Malviya, Manisha
Sirari, Titiksha
Sihag, Bhupendra
Saini, Arushi
Jyothi, Vishalavath
Sankhyan, Naveen
Source :
Journal of Pediatric Neurosciences; Jul-Sep2021, Vol. 16 Issue 3, p206-211, 6p
Publication Year :
2021

Abstract

Background: X-linked dystrophinopathies have a wide spectrum of manifestation. The most common forms are severe Duchenne muscular dystrophy (DMD) and Becker's muscular dystrophy (BMD). However, less common manifestations are isolated cardiomyopathy, myalgia, cramps, rhabdomyolysis, hyperCKemia, and manifest female carriers. Materials and Methods: This case series is a part of an ongoing long-term prospective cohort of children with DMD and BMD from the year 2013. The clinical details are maintained in the clinic files and standard management protocols are followed. For this case series, clinical details were collected from the clinic files and recorded on a case record proforma. Details of cardiology, radiology, and genetic investigations were collected. Results: We report cases of classical DMD, BMD, manifest female carrier with proximal pelvic girdle weakness, a female carrier with isolated dilated cardiomyopathy, and infantile-onset asymptomatic hyperCKemia. We also report less common but notable clinical presentations of DMD, autism, intellectual disability, epilepsy, and asymptomatic transaminitis. Conclusions: It is important for clinicians to be aware of these less common clinical presentations for prompt diagnosis, and to avoid unnecessary investigations. Here, we report the clinical spectrum of dystrophinopathies seen in pediatric neuromuscular clinic and emphasize the variability and expanding knowledge about different manifestations of dystrophinopathies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18171745
Volume :
16
Issue :
3
Database :
Complementary Index
Journal :
Journal of Pediatric Neurosciences
Publication Type :
Academic Journal
Accession number :
157517709
Full Text :
https://doi.org/10.4103/jpn.JPN_89_20