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hereditary spastic paraplegia 29

MeSH: C536863ORPHA: 101009

Contents

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

Overview

hereditary spastic paraplegia that has material basis in variation in the chromosome region 1p31.1-p21.1

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 hereditary spastic paraplegia 29, sourced from HPO and Orphanet clinical annotations.

Lower limb hyperreflexiaBabinski signHearing impairmentPes cavusHiatus herniaHyperbilirubinemiaHerniaClonusImpaired vibratory sensationUpper limb hyperreflexiaAbnormality of the lower urinary tractSeizureAbnormal rectum morphologyImpaired proprioception

Classification & Codes

MeSH Code

C536863

Orphanet Code

ORPHA:101009
hereditary spastic paraplegia 29
MeSHC536863
OrphanetORPHA:101009
Treatments0 drug(s)
Symptoms on record14 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO