Table 2.
Diagnoses of patients undergoing Televisits (n = 1618)
| Diagnoses | n (%) |
|---|---|
| Departments of Clinical Neurosciences, of Diagnostics and Technology, and of Neurosurgery | 966 |
| Tumors | 161 (16.6) |
| Cerebrovascular diseases | 53 (5.5) |
| Headache | 120 (12.4) |
| Chiari malformation and syringomyelia | 42 (4.3) |
| Multiple sclerosis and related disorders | 77 (8.0) |
| Neurogenetic and neuromuscular disorders* | 249 (25.8) |
| Epilepsy and sleep disorders | 81 (8.4) |
| Dementias | 55 (5.7) |
| Parkinson and movement disorders | 93 (9.6) |
| Miscellaneous | 35 (3.6) |
| Department of Paediatric Neuroscience | 652 |
| Multiple sclerosis and related disorders | 10 (1.5) |
| Tourette Syndrome and other movement disorders | 64 (9.8) |
| Epilepsy | 195 (29.9) |
| Neurogenetic and neuromuscular disorders** | 128 (19.6) |
| Cerebral Palsy | 51 (7.8) |
| Neurodevelopmental disorders*** | 90 (13.8) |
| Language or/and learning disorders | 81 (12.4) |
| Tumors and cerebrovascular disease | 14 (2.2) |
| Neurocutaneous diseases | 11 (1.7) |
| Craniostenosis syndrome and Chiari malformation | 8 (1.2) |
*Neuropathies, ataxias, spastic paraplegias, Huntington’s chorea, mitochondrial and neurometabolic disorders, myopathies, myasthenia gravis, amyotrophic lateral sclerosis
**Neuropathies, ataxias, spastic paraplegias, mitochondrial and neurometabolic disorders, myopathies, myasthenia gravis, spinal muscular atrophy
***Genetic syndromes, global delay, intellectual disability, and autism spectrum disorders