Abstract
After submitting a typical case of Anderson-Fabry disease in a 38 years old male, we discuss the eminent aspects of this metabolic disorder and, above all, the clinical, biochemical and ultrastructural problems of diagnosis in the heterozygotic relatives.
| Original language | English |
|---|---|
| Pages (from-to) | 123-134 |
| Journal | Medicina cutánea ibero-latino-americana |
| Volume | 15 |
| Issue number | 2 |
| Publication status | Published - 1 Jan 1987 |