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Autosomal recessive spastic paraplegia type 67

MONDO:0018419

Autosomal recessive spastic paraplegia type 67 is an extremely rare, complex hereditary spastic paraplegia characterized by an infancy or childhood onset of global developmental delay and progressive spasticity with tremor in the distal limbs, increased deep tendon reflexes and extensor plantar responses, which may be associated with mild intellectual disability. Additional features include muscle wasting and cerebellar abnormalities.

Also known as: SPG67

14 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Neuromuscular disease (98) Central nervous system disorder (97) Paraplegia (37) Palsy (29) Syndromic disease (24) Hereditary spastic paraplegia (21)

Trials to join now! 5 Not yet recruiting 2 Not yet finished but already full! 2 Completed 5

Autosomal recessive spastic paraplegia type 67

Broader categories

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