Spinal Muscular Atrophy (SMA): Difference between revisions
Evelin Milev (talk | contribs) No edit summary |
Evelin Milev (talk | contribs) No edit summary |
||
Line 6: | Line 6: | ||
== Introduction == | == Introduction == | ||
Spinal Muscular Atrophy (SMA) is a genetic condition | Spinal Muscular Atrophy (SMA) is a genetic condition under the scope of the neuromuscular disorders. It is characterised by degeneration of alpha motor neurons in the spinal cord. | ||
Spinal Muscular Atrophy affects ... | Spinal Muscular Atrophy affects ... |
Revision as of 15:04, 11 June 2018
Original Editor - Your name will be added here if you created the original content for this page.
Lead Editors
Introduction[edit | edit source]
Spinal Muscular Atrophy (SMA) is a genetic condition under the scope of the neuromuscular disorders. It is characterised by degeneration of alpha motor neurons in the spinal cord.
Spinal Muscular Atrophy affects ...
Clinically Relevant Anatomy
[edit | edit source]
add text here relating to clinically relevant anatomy of the condition
Mechanism of Injury / Pathological Process
[edit | edit source]
add text here relating to the mechanism of injury and/or pathology of the condition
Clinical Presentation[edit | edit source]
add text here relating to the clinical presentation of the condition
Diagnostic Procedures[edit | edit source]
add text here relating to diagnostic tests for the condition
Outcome Measures[edit | edit source]
add links to outcome measures here (see Outcome Measures Database)
Management / Interventions
[edit | edit source]
add text here relating to management approaches to the condition
Differential Diagnosis
[edit | edit source]
add text here relating to the differential diagnosis of this condition
Resources
[edit | edit source]
add appropriate resources here