A 27-year-old female, diagnosed with PE at the age of 25 years, studied with enzyme levels due to maternal history of Fabry.
It begins at 16 years of age episodes of intense colic abdominal pain not associated with food intake.
Subsequently, the patient presented pain episodes three times a month, moderate intensity and self-limiting.
No complications of PE, minimal angiokeratomas.
No enzyme replacement therapy.
No sensory symptoms.
The clinical and neurophysiological evaluation was normal.
