Other early-onset cerebellar ataxia
ICD-10 G11.19 is a billable code used to indicate a diagnosis of other early-onset cerebellar ataxia.
G11.19 refers to a category of hereditary and degenerative conditions characterized by early-onset cerebellar ataxia, which is a disorder that affects coordination and balance due to dysfunction of the cerebellum. This code encompasses various genetic and non-genetic conditions that manifest in childhood or early adulthood, leading to progressive motor impairment. Conditions such as spinocerebellar ataxias (SCAs), which are a group of inherited disorders, fall under this category. These ataxias can be caused by mutations in specific genes, leading to neuronal degeneration. Other hereditary conditions, such as Friedreich's ataxia, may also present with similar symptoms but are classified under different codes. The clinical presentation often includes gait instability, dysarthria, and oculomotor dysfunction. Diagnosis typically involves a combination of clinical evaluation, family history assessment, and genetic testing. The complexity of G11.19 arises from the need to differentiate it from other ataxias and motor neuron diseases, as well as the requirement for thorough documentation to support the diagnosis.
Comprehensive neurological examination findings, family history, and results from genetic testing.
Patients presenting with gait disturbances, coordination issues, and family history of ataxia.
Neurologists should ensure that all relevant diagnostic tests are documented to support the diagnosis.
Detailed genetic testing results, family pedigree charts, and clinical assessments.
Patients referred for genetic counseling due to family history of ataxia or related disorders.
Geneticists must provide clear documentation linking genetic findings to clinical symptoms.
Used to assess cognitive function in patients with ataxia.
Detailed report of cognitive assessments and interpretations.
Neurologists should ensure that cognitive assessments are linked to the diagnosis of ataxia.
G11.19 is used for other types of early-onset cerebellar ataxia that do not fit the specific criteria for Friedreich's ataxia (G11.0). It is important to document the specific type of ataxia to ensure accurate coding.
