hereditary disease atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome https://www.malacards.org/card/atherosclerosis_deafness_diabetes_epilepsy_nephropathy_syndrome https://www.malacards.org/card/atherosclerosis_premature_with_deafness_nephropathy_diabetes_mellitus_photomyoclonus_and_degenerative_neurologic_disease GARD:0002279 MESH:C565928 SCTID:720519003 premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder MONDO:0008843 Feigenbaum-Bergeron-Richardson syndrome Orphanet:1192 Feigenbaum Bergeron Richardson syndrome MEDGEN:349198 A rare, severe, circulatory system disease characterized by premature, diffuse, severe atherosclerosis (including the aorta and renal, coronary, and cerebral arteries), sensorineural deafness, diabetes mellitus, progressive neurological deterioration with cerebellar symptoms and photomyoclonic seizures, and progressive nephropathy. Partial deficiency of mitochondrial complexes III and IV in the kidney and fibroblasts (but not in muscle) may be associated. There have been no further descriptions in the literature since 1994. OMIM:209010 UMLS:C1859596 epilepsy syndrome