1, progressive supranuclear ophthalmoplegia (1)]. The ICD-9 (used previously in the United States) did not have a specific code for PSP; instead, the code 333.0 (other degenerative diseases of the basal ganglia) (27) was primarily used to document PSP.Jun 17, 2021
What is progressive supranuclear palsy (PSP)?
Progressive supranuclear palsy (PSP) is a rare progressive brain disorder that affects movement, gait, eye movements, speech, and cognition.
What is the ICD 10 code for Bell's palsy?
ICD-10-CM Diagnosis Code G23.1. Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] 2016 2017 2018 2019 2020 2021 Billable/Specific Code. Applicable To. Progressive supranuclear palsy. ICD-10-CM Diagnosis Code G51.0 [convert to ICD-9-CM] Bell's palsy. Bell's palsy of left face; Bell's palsy of right face; Bells palsy;
What is progressive supranuclear ophthalmoplegia?
Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski] A rare neurodegenerative disorder characterized by gait and balance difficulties and loss of coordination of eye movements. Progressive supranuclear palsy (psp) is a rare brain disease. It affects brain cells that control the movement of your eyes.
What is the ICD-9 code for diagnosis?
ICD-9-CM 333.0 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 333.0 should only be used for claims with a date of service on or before September 30, 2015.
What is progressive supranuclear palsy?
Progressive supranuclear palsy (psp) is a rare brain disease. It affects brain cells that control the movement of your eyes.
Why is PSP dangerous?
However, psp is dangerous because it increases your risk of pneumonia and choking from swallowing problems and injuries from falling. Spastic weakness of the muscles innervated by the cranial nerves, i.e., the muscle of the face, pharynx, and tongue, due to bilateral lesions of the corticospinal tract.
What is the degenerative disorder of the central nervous system?
A degenerative disease of the central nervous system characterized by balance difficulties; ocular motility disorders (supranuclear ophthalmoplegia); dysarthria; swallowing difficulties; and axial dystonia. Onset is usually in the fifth decade and disease progression occurs over several years.
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