autosomal recessive spastic paraplegia type 67

ORPHA: 401820

Contents

1. Overview
2. Available Treatments
3. Clinical Presentation
4. Classification & Codes

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 autosomal recessive spastic paraplegia type 67, sourced from HPO and Orphanet clinical annotations.

Mild intellectual disabilityGlobal developmental delayAgenesis of corpus callosumGait disturbanceHyperreflexiaLower limb spasticitySpastic gaitCerebral cortical atrophyBabinski signGeneralized amyotrophyAplasia/Hypoplasia of the cerebellar vermisProgressive spastic paraplegiaAbnormal myelinationAbnormality of movementLimb tremor

Classification & Codes

Orphanet Code

ORPHA:401820

autosomal recessive spastic paraplegia type 67

Orphanet	`ORPHA:401820`
Treatments	0 drug(s)
Symptoms on record	15 signs
Status	published

Factual Authority

Last Updated3/20/2026

Clinical DataHPO · Orphanet

Drug DataFDA · EMA · CDSCO