| Literature DB >> 28503602 |
Inaam Noureldyme Mohamed1, Maha Abdelmoneum Elseed1, Ahlam Abdalrhman Hamed1.
Abstract
BACKGROUND: There is no available data from Sudan reflecting the magnitude of the neurological disorders and disabilities in the pediatric age-group. This study aims to evaluate the pattern of neurological disorders among Sudanese children. PATIENTS AND METHODS: This is a retrospective survey of children with epilepsy and other neurodisability disorders seen at pediatric neurology outpatient clinic, during the period from January 2007 to August 2013. The data of 9600 patients were analyzed.Entities:
Keywords: children; disorders; neurological
Year: 2016 PMID: 28503602 PMCID: PMC5417275 DOI: 10.1177/2329048X15623548
Source DB: PubMed Journal: Child Neurol Open ISSN: 2329-048X
Cost of the Commonly Used Investigations.
| Investigations | Cost (Sudanese Geneh) (US Dollar) |
|---|---|
| Computed tomography scans | 200 (22) |
| Magnetic resonance imaging of the brain with contrast | 800 (88) |
| Magnetic resonance imaging of the spine with contrast | 800 (88) |
| Magnetic resonance angiography | 600 (66) |
| Magnetic resonance spectroscopy | 500 (55) |
| Magnetic resonance venography | 500 (55) |
| Electroencephalography | 250 (28) |
| Electromyography | 600 (66) |
| Nerve conduction studies | 600 (66) |
| Metabolic screen | 1500 (166) |
Pattern of Neurological Disorder in Sudanese Children.
| Disorders | Number (%) |
|---|---|
| Seizure disorders | 2877 (47.7) |
| Cerebral palsy | 1149 (19.1) |
| Congenital anomalies of the central nervous system | 337 (05.6) |
| Muscular disorders | 192 (3.2) |
| Neurodegenerative brain diseases. | 180 (3.0) |
| Spinal cord pathology (spinal schistosomiasis) | 132 (2.2) |
| Acute demyelinating disorders | 126 (2.1) |
| Acute stroke | 114 (1.7) |
| Ataxia | 114 (1.7) |
| Behavioral problems | 100 (1.5) |
| Myasthenia Gravis | 72 (1.2) |
| Genetic syndromesa | 70 (1.2) |
| Brain tumors | 65 (1.1) |
| Neurocutaneous syndromes | 55 (1.0) |
| Guillain-Barre syndrome | 55 (1.0) |
| Mitochondrial disorders | 50 (0.7) |
| Nonepileptic paroxysmal disorders | 50 (0.7) |
| Movement disorders | 50 (0.7) |
| Charcot-Marie-Tooth disease | 26 (0.5) |
| Metabolic disorders | 26 (0.5) |
| Idiopathic intracranial hypertension | 10 (0.3) |
| headache and migraine | 10 (0.3) |
| Miscellaneousb | 100 (1.6) |
| Could not be placed in a diagnostic categoryc | 89 (1.4) |
| Total | 6019 (100) |
aIncludes patients with dysmorphic features and obvious syndromic diagnoses that were clinically identified but could not be proved due to lack of local genetic services.
bInclude patients with Bell’s palsy, Abducens/Trochlear nerve palsies, headache, migraine, nocturnal enuresis, learning difficulties (dyslexia and others), intracranial calcifications (TORCH and pseudo TORCH and others), systemic lupus erythematosus vasculitis, some rare disorders, for example, Stiffman syndrome, dysautonomia, hyperekplexia, chronic infantile neurological cutaneous articular syndrome.
cThis group of patients has rare disorders that cannot be placed in any of the above mentioned categories needing further genetic and/ or metabolic workup which are not available in our setup. Some proved to have novel genes (under publication). Abbreviations: TORCH, Toxoplasmosis, Rubella, Cytomegalovirus, Herpes Simplex.