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Quadriplegia
Paralysis affecting all 4 limbs.
Synonym: Tetraplegia
Partial loss of power is Quadriperesis/tetraperesis
Types: I. Quadriplegia of upper motor Neuron Lesion
II. Quadriplegia of lower motor neuron lesion.
II. Lower motor lesion: Flaccid quadriplegia
CLASSIFICATION (According to the site of lesion)
SITES:
Anterior horn cells/Roots/peripheral nerves/Myoneuronal junction/Muscles.
✿Lesions of anterior horn cells:
Acute anterior Poliomyelitis
✿Lesions of Roots:
Guillain-Barre Syndrome
✿Lesions of Peripheral Nerves
Polyneuropathy
✿Lesions of myoneuronal junction:
Myasthenia gravis
✿Lesions of Muscles:
Myopathy
a) Genetic
b) Non genetic
Periodic paralysis
Spastic Quadriplegia
Sites of Lesion:
High cervical cord/Brain stem/Cortex
QuadriplegiaPredominantly involving proximal group of muscles
Conditions causing:
1. Poliomyelitis –Anterior horn cells
2. Spinal muscular atrophy
genetically determined disease of motor neurons
3. Guillain –Barre Syndrome(GBS)
4. Periodic paralysis, Myotonia
5. Myopathy
6. Myasthenia
7. Diabetic Mononeuritis multiplex
(Sciatic and femoral nerve)
8. Diabetic myopathy
-involving proximal shoulder, pelvic girdle muscles
-unilaterally or bilaterally.
Predominantly involving distal group of muscles
1. Distal Myopathies
2. Peroneal muscular atrophy.
3. Polyneuropathies.
-Multiple symmetrical peripheral neuropathies
(Alcoholism, diabetes, carcinoma, lead poisoning)
4. Mononeuritis multiplex
-Asymmetrical involvement of peripheral nerves.
(-Leprosy, Amyloid, PNA, neurofibroma)
Differential Diagnosis of Quadriplegia.
I. AS PER NEURO ANATOMICAL SITE OF LESION
II. TENDON REFLEXES AND QUADRIPLEGIA
III.Diagnosis according to chronological evolution
2. Diphtheria
3. Porphyria
4. Toxic neuropathy.
5. Rarely- myasthenia
6. Toxic myopathy.
7. Endocrine myopathy.
IV. Diagnosis according to progression of the disability
i) Over weeks to months
Polymyositis, Dermato myositis.
ii) Over years
Spinal muscular atrophy
(Werdnig- HoffmanSyndrome, Kugleberg welander
Syndrome)
Myasthenia
Muscular dystrophies.
Anterior horn cell Disease.
Less common- Myopathy
Oculopharyngeal
Polymyositis.
Dermato myositis.
Congenital myopathy - rare
-Distal weakness along with proximal.
V. Differentiation by certain presentations
Never in M.N.D./peripheral neuropathy / Eaton Lambert’s-no ocular or bulbar involvement.
Myasthenia, Myotonia.
Others:- Oculo pharyngeal dystrophy
Diabetes with Mononeuritis multiplex.
Progressive external ophthalmoplegia
Kearns –Sayer Syndrome.
d. Episodic Weakness
Periodic paralysis
Myasthenia Gravis
Eaton-Lambert’s Syndrome-No weakness of ocular /bulbar muscles.
Recurrent temporary flaccid paralysis.
7. Hypothyroidism/ Hyperthyroidism
8. Porphyria
/Spinal cord lesion/ Brain stem lesions/cerebrallesions
Spastic diplegia-All 4 limbs are affected but lower limbs are affected more than upper limbs.
ASSESSMENT
Depends on site of suspected pathology
TREATMENT:
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