Talk:Musculoskeletal System Development
From Embryology
Muscle Abnormalities
Clinical heterogeneity of duchenne muscular dystrophy (DMD): definition of sub-phenotypes and predictive criteria by long-term follow-up. Desguerre I, Christov C, Mayer M, Zeller R, Becane HM, Bastuji-Garin S, Leturcq F, Chiron C, Chelly J, Gherardi RK. PLoS One. 2009;4(2):e4347. Epub 2009 Feb 5. PMID: 19194511 | PLoS
DMD can be divided into 4 sub-phenotypes differing by severity of muscle and brain dysfunction. Simple early criteria can be used to include patients with similar outcomes in future therapeutic trials.
- A (early infantile DMD, 20%): severe intellectual and motor outcomes
- B (classical DMD, 28%): intermediate intellectual and poor motor outcome
- C (moderate pure motor DMD, 22%): normal intelligence and delayed motor impairment
- D (severe pure motor DMD, 30%)