juvenile amyotrophic lateral sclerosis

ORPHA: 300605

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 juvenile amyotrophic lateral sclerosis, sourced from HPO and Orphanet clinical annotations.

Muscle weaknessLower limb spasticitySkeletal muscle atrophyDistal amyotrophyUpper limb spasticityAmyotrophic lateral sclerosisSpastic diplegiaHypertoniaGait disturbanceDystoniaBrisk reflexesAbnormal speech patternDistal muscle weaknessBulbar signsInability to walkCNS hypomyelinationLower-limb joint contractureDelayed ability to walkArm dystoniaMuscle fiber atrophyUpper-limb joint contractureUrinary incontinenceMicrocephalySupranuclear gaze palsyNystagmusAtypical behaviorAtaxiaGlobal developmental delayParkinsonismAbnormal cerebellum morphologyDysphagiaChoreaClonusOpisthotonusAnarthriaAxial dystoniaRetrocollisHead titubationScoliosisProximal muscle weaknessNeck flexor weaknessCachexiaGastrostomy tube feeding in infancyOromandibular dystoniaTip-toe gaitCognitive impairment

Classification & Codes

Orphanet Code

ORPHA:300605
juvenile amyotrophic lateral sclerosis
OrphanetORPHA:300605
Treatments0 drug(s)
Symptoms on record46 signs
Statuspublished
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO