Duchenne muscular dystrophy in a Filipino boy reaching adulthood, and nine years into oral corticosteroids: A case report
10.35460/2546-1621.2023-0022
- Author:
Erwin Damian V. Marcelo
1
;
Raymond L. Rosales
1
,
2
Author Information
1. Department of Internal Medicine, Metropolitan Medical Center
2. Center for Neurodiagnostic and Therapeutic Services, Metropolitan Medical Center
- Publication Type:Other Types
- Keywords:
Progressive muscle weakness;
DMD
- MeSH:
Dystrophin;
Mortality, Premature
- From:
Journal of Medicine University of Santo Tomas
2023;7(1):1181-1185
- CountryPhilippines
- Language:English
-
Abstract:
Rationale:Duchenne muscular dystrophy (DMD) is a disease that primarily manifests in the early stages of life and progressively affects muscle strength resulting in quadriparesis and ultimately resulting in premature death secondary to cardiac or respiratory failure. DMD is the most common x-linked genetic disorder in children that is because of an alteration of a protein called “dystrophin” which is responsible for strengthening muscle fibers and protecting them from injury as muscles contract and relax.
Objective:To highlight the case of a 19-year-old male who was diagnosed with DMD at 8 years of age and treated with oral corticosteroid and rehabilitation.
Case:We present the case of a 19-year-old male who developed difficulty climbing stairs and was diagnosed with DMD at 8 years old with the use of clinical exome sequencing. Corticosteroid therapy was initiated and rehabilitation perpetuated which dramatically improved his life expectancy.
Discussion and Summary:Clinical exome sequencing was employed on our patient to confirm the diagnosis of DMD from other neuromuscular and neurodegenerative diseases. Most cases of DMD succumb to cardiopulmonary arrest before reaching adulthood; however, this case exemplifies DMD from other cases since our patient was able to prolong his life with continuation of oral corticosteroid and rehabilitation and in the absence of extensive life support.
- Full text:jmust 13.pdf