PedAM
Pediatric Disease Annotations & Medicines
| Disease | neuropathy |
| Phenotype | C0037773|hereditary spastic paraplegia |
| Sentences | 2 |
| PubMedID- 22192498 | Peripheral neuropathy in hereditary spastic paraplegia due to spastin (spg4) mutation--a neurophysiological study using excitability techniques. |
| PubMedID- 25008398 | Objective: to establish the phenotypic spectrum of kif5a mutations and to investigate whether kif5a mutations cause axonal neuropathy associated with hereditary spastic paraplegia (hsp) or typical charcot-marie-tooth disease type 2 (cmt2). |
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