Huntington disease-like 1

MeSH: C566398ORPHA: 157941

Overview

human disease

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 Huntington disease-like 1, sourced from HPO and Orphanet clinical annotations.

ChoreaAtypical behaviorDepressionDementiaDelusionDysarthriaGait disturbanceGait ataxiaVentriculomegalyInvoluntary movementsCognitive impairmentMask-like faciesAbnormality of eye movementSlow saccadic eye movementsAbnormal saccadic eye movementsAbnormality of ocular smooth pursuitNystagmusRestlessnessDelayed speech and language developmentSeizureCerebellar atrophyGeneralized hypotoniaDysmetriaSlurred speechWeight lossBradykinesiaCerebral cortical atrophyAbnormal basal ganglia morphologyGliosisIncoordinationClumsinessEEG abnormalityMemory impairmentFrequent fallsHypokinesiaAbnormal head movementsAbnormal posturingAbnormal shoulder morphologyHyperactive deep tendon reflexesJerky head movementsPoor fine motor coordinationJerky ocular pursuit movementsAbnormality of mental functionSimultanapraxia

Classification & Codes

MeSH Code

C566398

Orphanet Code

ORPHA:157941
Huntington disease-like 1
MeSHC566398
OrphanetORPHA:157941
Treatments0 drug(s)
Symptoms on record44 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO