Gerstmann-Straussler-Scheinker syndrome is a rare, inherited prion disease characterized by progressive neurodegeneration. It is caused by the accumulation of abnormal prion proteins in the brain, leading to severe neurological symptoms. Accurate coding with ICD-10 Code A81.82 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that healthcare providers can effectively manage and track this condition.
ICD-10 Code A81.82 represents Gerstmann-Straussler-Scheinker syndrome, a genetic prion disease that leads to progressive neurological decline. This code should be used in clinical documentation and billing when diagnosing patients with this condition, ensuring accurate representation of the disease for treatment planning and healthcare statistics.
Gerstmann-Straussler-Scheinker syndrome is caused by mutations in the prion protein gene, leading to the accumulation of misfolded proteins in the brain. The condition progresses over time, resulting in severe cognitive and motor impairments, necessitating medical attention.
ICD-10 Code A81.82 is utilized in SOAP notes to document the presence of Gerstmann-Straussler-Scheinker syndrome. It aids in capturing symptoms, assessments, and treatment plans, relevant in both acute and chronic care settings.
In SOAP notes, ICD-10 Code A81.82 connects subjective reports of symptoms and objective clinical findings to a formal diagnosis of Gerstmann-Straussler-Scheinker syndrome. This ensures continuity of care, supports billing, and meets EHR documentation standards.
Gerstmann-Straussler-Scheinker syndrome requires urgent medical attention due to its progressive nature. Treatment focuses on managing symptoms and providing supportive care.
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CPT Code | Description |
---|---|
99214 | Established patient office visit, moderate complexity. |
93000 | Electrocardiogram, ECG, with interpretation and report. |
70450 | CT scan of the head or brain. |
96136 | Psychological testing evaluation. |
Common Questions About Using ICD-10 Code A81.82 for Gerstmann-Straussler-Scheinker syndrome
What are the common symptoms of Gerstmann-Straussler-Scheinker syndrome?
Common symptoms include progressive cognitive decline, ataxia, myoclonus, and seizures. Patients may also experience visual disturbances and other neurological impairments as the disease progresses.
How is Gerstmann-Straussler-Scheinker syndrome diagnosed?
Diagnosis is typically made through clinical evaluation, family history assessment, and neuroimaging studies. Genetic testing may also be performed to confirm mutations associated with prion diseases.
Is Gerstmann-Straussler-Scheinker syndrome contagious?
No, Gerstmann-Straussler-Scheinker syndrome is not contagious. It is a genetic disorder caused by mutations in the prion protein gene and is not transmitted from person to person.
What treatment options are available for Gerstmann-Straussler-Scheinker syndrome?
There is no cure for Gerstmann-Straussler-Scheinker syndrome. Treatment focuses on managing symptoms and providing supportive care, including physical therapy and nutritional support.
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