Hereditary cerebrovascular diseases
ICD-10 I67.85 is a used to indicate a diagnosis of hereditary cerebrovascular diseases.
Hereditary cerebrovascular diseases encompass a range of genetic conditions that predispose individuals to cerebrovascular disorders, including strokes and vascular malformations. Clinically, patients may present with recurrent headaches, transient ischemic attacks (TIAs), or strokes at a younger age than typically expected. The anatomy involved primarily includes the cerebral arteries and veins, which may be structurally abnormal due to genetic mutations affecting vascular integrity. Disease progression can vary widely; some patients may experience early onset of cerebrovascular events, while others may remain asymptomatic for years. Diagnostic considerations include a thorough family history, imaging studies such as MRI or CT angiography to identify vascular anomalies, and genetic testing to confirm hereditary conditions. It is crucial to differentiate hereditary cerebrovascular diseases from acquired conditions to ensure appropriate management and counseling.
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
Standard ICD-10-CM documentation requirements apply
Various clinical presentations within this specialty area
Follow specialty-specific billing guidelines
I67.85 covers hereditary conditions such as CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy), Fabry disease, and other genetic syndromes that lead to cerebrovascular complications.
I67.85 should be used when there is clear evidence of a hereditary condition contributing to cerebrovascular disease, particularly when genetic testing confirms the diagnosis or when there is a significant family history of similar conditions.
Documentation should include a detailed family history of cerebrovascular diseases, results from genetic testing, imaging studies showing vascular abnormalities, and clinical notes outlining the patient's symptoms and progression.
