Progressive bulbar palsy (Q41048): Difference between revisions

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+August 2026Timestamp +2026-08-13T00:00:00Z
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+G12.2
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Latest revision as of 07:06, 13 August 2026

Progressive bulbar palsy (PBP) is a variant of amyotrophic lateral sclerosis that initially presents with symptoms of bulbar weakness such as dysarthria and dysphagia. Symptoms may remain relatively confined to the bulbar region. PBP more commonly affects females than males. Patients typically progress to develop limb weakness and features consistent with more typical ALS at a later stage of disease.

Language	Label	Description	Also known as
default for all languages	8B60.1
English	Progressive bulbar palsy	Progressive bulbar palsy (PBP) is a variant of amyotrophic lateral sclerosis that initially presents with symptoms of bulbar weakness such as dysarthria and dysphagia. Symptoms may remain relatively confined to the bulbar region. PBP more commonly affects females than males. Patients typically progress to develop limb weakness and features consistent with more typical ALS at a later stage of disease.