| Image = | Caption = | DiseasesDB = | ICD10 = | ICD9 = | ICDO = | OMIM =
| MedlinePlus = | eMedicineSubj = | eMedicineTopic = | MeshName =
Juvenile+Primary+Lateral+Sclerosis | MeshNumber = |
}}Juvenile primary lateral sclerosis (JPLS) ,also known as as primary
lateral sclerois (PLSJ), is a rare genetic disorder, with a small number
of reported cases, characterized by progressive weakness and stiffness of
muscles in the arms, legs, and face. This disorder damages motor neurons,
which are specialized nerve cells in the brain and spinal cord that
control muscle movement.
Symptoms and progression
Symptoms of JPLS begin in early childhood and progress over a period of 15
to 20 years. Early symptoms include clumsiness, muscle spasms, weakness and
stiffness in the legs, and difficulty with balance. As symptoms progress,
they include we
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