
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Duchenne muscular dystrophy diagnostic study of choice
Introduction
Overview
Overview
Genetic analysis is the gold standard test for the diagnosis of Duchenne muscular dystrophy.
Diagnostic Study of Choice
Diagnostic Study of Choice
Study of choice
Genetic analysis is the gold standard test for the diagnosis of Duchenne muscular dystrophy.
Investigations:
- Among the patients who present with clinical signs of Duchenne muscular dystrophy, the CK level is the most sensitive test for the diagnosis.
- Among the patients who present with clinical signs of Duchenne muscular dystrophy, the genetic analysis is the most specific test for diagnosis.
Diagnostic results
The following finding on performing genetic analysis is confirmatory for Duchenne muscular dystrophy:
- Different mutations such as deletion, duplication, and etc in dystrophin gene.
Sequence of Diagnostic Studies
The various investigations must be performed in the following order:
- History and physical examination
- CK level
- Genetic analysis
- Muscle biopsy (if genetic analysis in negative)
Name of Diagnostic Criteria
Duchenne muscular dystrophy is primarily diagnosed based on clinical presentation and genetic testing. There are no established criteria for the diagnosis of Duchenne muscular dystrophy.
References
References
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.
