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Written by Administrator
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Friday, 04 February 2011 05:25 |
Examination for signs of proximal muscle weakness includes:
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Watching for abdominal breathing or accessory muscle use
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Evaluating for head lag when pulled to sit (also note biceps resistance- failure of child pulling back when pulled to sit)- or inability to voluntarily flex neck when supine
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Evaluating whether child “slips through the hands” when held suspended (examiner’s hands under the armpits)
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Stimulating foot and evaluate force of withdrawal movement
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Watching for difficulty rising from floor (including Gowers maneuver, full or modified)
On exam, look for muscle hypertrophy or atrophy, particularly calves and tongue (calves may also feel abnormally full).
See the “Motor Assessment by Age” surveillance aid for more information.
Other physical findings may help distinguish neuromuscular disease (peripheral cause, such as Duchenne muscular dystrophy) from diseases of the brain (central cause, such as cerebral palsy), as shown in the table that follows. The table that follows shows general guidelines, though evaluation requires use of clinical judgment related to the child’s overall developmental history.
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Sign |
Peripheral Cause |
Central Cause |
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Chest size |
May be small with bell shape |
Usually normal |
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Facial movement |
Often weak “myopathic” with high arched palate |
Usually normal |
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Tongue fasciculation |
May be present, particularly in SMA |
Absent |
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Tone |
Reduced tone |
Reduced tone or increased tone with scissoring |
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Deep Tendon Reflexes |
Decreased or absent |
Increased, may have clonus |
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Gait |
Toe walking
Waddling
Hyperlordotic
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Toe walking
Hemiparetic
Spastic
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To view Peripheral signs of weakness click here.
It is important to test for signs of motor weakness over time. If a child does not achieve a motor milestone at the expected time, follow up until the milestone is achieved, or until there is sufficient concern or referral. Ask about and evaluate for signs of motor regression.
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Last Updated on Thursday, 30 August 2012 15:39 |