ICD-10 Code E75.21 | Fabry (-Anderson) disease Symptoms, Diagnosis, Billing

Common symptoms include episodes of pain in the hands and feet, skin lesions known as angiokeratomas, gastrointestinal issues, and progressive renal impairment. Early recognition of these symptoms is crucial for timely diagnosis and management.

Diagnosis typically involves clinical evaluation, family history assessment, and laboratory tests to measure alpha-galactosidase A enzyme activity. Genetic testing may also be performed to confirm the diagnosis.

While there is no cure for Fabry (-Anderson) disease, treatment options such as enzyme replacement therapy can help manage symptoms and prevent complications. Supportive care is also essential for improving quality of life.

Genetic counseling is important for affected individuals and their families to understand the inheritance pattern, implications for family planning, and available testing options for at-risk relatives.