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1 OMIM reference -
2 associated genes
16 signs/symptoms
COMMON GENES: 1
COMMON SIGNS: 11
3 OMIM references -
4 associated genes
12 signs/symptoms
Juvenile primary lateral sclerosis
Juvenile amyotrophic lateral sclerosis

ALS2 ALS2
ERLIN2 FUS
SIGMAR1
SPG11


COMMON
GENES
ALS2



Citations in the biomedical literature:


Juvenile primary lateral sclerosis
ALS2 ERLIN2
Juvenile amyotrophic lateral sclerosis
FUS SIGMAR1 SPG11



Juvenile primary lateral sclerosis
Juvenile amyotrophic lateral sclerosis

Synonym(s):
- JPLS
- Juvenile PLS

Synonym(s):
- JALS
- Juvenile Charcot disease
- Juvenile Lou Gehrig disease

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: any age
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: adult
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C536416
External references:
3 OMIM references -
No MeSH references


COMMON
SIGNS
- Abnormal gait
- Autosomal recessive inheritance
- Bladder and ureter anomalies
- Elocution disorders / dysarthria / dysphonia
- Hypereflexia
- Hypertonia / spasticity / rigidity / stiffness
- Motor deficit / trouble
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Pseudobulbar signs / spasmodic laugh and cry
- Pyramidal syndrome
- Sensitive trouble / deficit


Juvenile primary lateral sclerosis
Juvenile amyotrophic lateral sclerosis

Very frequent
- Ataxia / incoordination / trouble of the equilibrium
- Hemiplegia / diplegia / hemiparesia / limb palsy
- Muscle weakness / flaccidity

Frequent
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia



Very frequent
- Abnormal EMG / electromyogram / electropmyography