Table 1

Characteristics of 20 patients with bilateral Horner’s syndrome

PatientSexAgeDiagnosis
1F17Hereditary sensory and autonomic neuropathy (HSAN), Type III
2F57Amyloidosis
3F58Amyloidosis
4M70Amyloidosis
5F52Amyloidosis
6M37Anderson-Fabry disease
7M58Diabetes mellitus
8M54Diabetes mellitus
9F39Diabetes mellitus
10M18Familial dysautonomia
11M67Multiple system atrophy
12M30Pure autonomic failure
13M59Pure autonomic failure
14M50Pure autonomic failure
15M52Pure autonomic failure
16F35Dopamine-β-hydroxylase deficiency
17M40Dopamine-β-hydroxylase deficiency
18F52Carcinomatous sympathetic neuropathy
19F49Spinal artery thrombosis
20F74Bilateral cervical sympathectomy