Idiopathic small fiber neuropathy: phenotype, etiologies, and the search for fabry disease.

[fabry disease]

The etiology of small fiber neuropathy (SFN ) often remains unclear . Since SFN may be the only symptom of late-onset Fabry disease , it may be underdiagnosed in patients with idiopathic polyneuropathy . We aimed to uncover the etiological causes of seemingly idiopathic SFN by applying a focused investigatory procedure , to describe the clinical phenotype of true idiopathic SFN , and to elucidate the possible prevalence of late-onset Fabry disease in these patients .Forty -seven adults younger than 60 years with seemingly idiopathic pure or predominantly small fiber sensory neuropathy underwent a standardized focused etiological and clinical investigation . The patients deemed to have true idiopathic SFN underwent genetic analysis of the alpha-galactosidase A gene (GLA ) that encodes the enzyme alpha-galactosidase A (Fabry disease ).The following etiologies were identified in 12 patients : impaired glucose tolerance (58 .3 %), diabetes mellitus (16 .6 %), alcohol abuse (8 .3 %), mitochondrial disease (8 .3 %), and hereditary neuropathy (8 .3 %). Genetic alterations of unknown clinical significance in GLA were detected in 6 of the 29 patients with true idiopathic SFN , but this rate did not differ significantly from that in healthy controls (n =203 ). None of the patients with genetic alterations in GLA had significant biochemical abnormalities simultaneously in blood , urine , and skin tissue .A focused investigation may aid in uncovering further etiological factors in patients with seemingly idiopathic SFN , such as impaired glucose tolerance . However , idiopathic SFN in young to middle -aged Swedish patients does not seem to be due to late-onset Fabry disease .

Diseases
Validation

Diseases presenting "diabetes mellitus" symptom

acute rheumatic fever

adrenal incidentaloma

adrenomyeloneuropathy

allergic bronchopulmonary aspergillosis

alpha-thalassemia

child syndrome

cholangiocarcinoma

cohen syndrome

congenital adrenal hyperplasia

congenital toxoplasmosis

cowden syndrome

cushing syndrome

cystinuria

esophageal adenocarcinoma

esophageal carcinoma

esophageal squamous cell carcinoma

fabry disease

familial hypocalciuric hypercalcemia

malignant atrophic papulosis

neuralgic amyotrophy

pyomyositis

sneddon syndrome

typhoid

werner syndrome

wolf-hirschhorn syndrome

This symptom has already been validated