spinocerebellar ataxia type 37
ORPHA: 363710
Overview
Spinocerebellar ataxia type 37 (SCA37) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1; see this term), characterized by a cerebellar syndrome along with altered vertical eye movements
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with spinocerebellar ataxia type 37, sourced from HPO and Orphanet clinical annotations.
Abnormal conjugate eye movementCogwheel rigidityFallsSensorineural hearing impairmentHorizontal nystagmusGait disturbanceMyoclonusTremorDysdiadochokinesisTruncal ataxiaAbnormal speech patternScanning speechLimb dysmetriaSomatic sensory dysfunctionCerebellar vermis atrophyDiffuse cerebellar atrophy
Classification & Codes
Orphanet Code
ORPHA:363710spinocerebellar ataxia type 37
| Orphanet | ORPHA:363710 |
| Treatments | 0 drug(s) |
| Symptoms on record | 16 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO