Spastic Paraplegia 3a

Alias:

Spastic Paraplegia 3

Spg3a

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraplegia, Hereditary

Spastic Paraplegia Type 3a

Atl1-Hsp

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Spastic Paraplegia 3a, also known as spastic paraplegia 3, is related to spastic paraplegia 31, autosomal dominant and neuropathy, and has symptoms including leg cramps, pain in lower limb and urgency of micturition. An important gene associated with Spastic Paraplegia 3a is ATL1 (Atlastin GTPase 1). The drugs Acetylcholine and Cholinergic Agents have been mentioned in the context of this disorder. Affiliated tissues include spinal cord and brain, and related phenotypes are adipose tissue and immune system

Related ID：

MALACARDS：SPS012