Description

Kaler et al compared general clinical features that can help distinguish between peripheral and central hypotonia. The authors are from Xavier University (Oranjestad), Franklin University and Windsor University.


Patient selection: motor delay

 

Parameters:

(1) social and cognitive status

(2) dysmorphic features

(3) hands

(4) tendon reflexes

(5) vertical suspension

(6) features of spinal dysraphism

(7) seizures

(8) history

(9) posture and spontaneous movement

(10) range of joint mobility

 

Parameter

Peripheral Hypotonia

Central Hypotonia

social and cognitive status

impaired

relatively normal

dysmorphic features

with organ malformation suggest a syndrome

myopathic facies

hands

fisting

 

tendon reflexes

normal or brisk

reduced or absent deep tendon jerks

vertical suspension

crossed adductor response or scissoring

reduced or absent spontaneous antigravity movements

signs of spinal dysraphism

may be present

absent

seizures

present

absent

history

hypoxic-ischemic encephalopathy, birth trauma, hypoglycemia

family history of neuromuscular disorders OR maternal myotonia

posture

 

frog-leg posture or jug-handle posture of arms; paucity of spontaneous movement

range of joint mobility

 

increased

 

where:

• Myopathic facies: open mouth with tented upper lip, poor lip seal when sucking, lack of facial expression, ptosis, restricted ocular movements


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