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1.
J Inherit Metab Dis ; 39(3): 465-466, 2016 05.
Article in English | MEDLINE | ID: mdl-27056553

ABSTRACT

Auditory impairment in mitochondrial disorders are usually due to peripheral sensorineural dysfunction. Central deafness is only rarely reported. We report here an 11-year-old boy with MELAS syndrome who presented with subacute deafness after waking up from sleep. Peripheral hearing loss was rapidly excluded. A brain MRI documented bilateral stroke-like lesions predominantly affecting the superior temporal lobe, including the primary auditory cortex, confirming the central nature of deafness. Slow recovery was observed in the following weeks. This case serves to illustrate the numerous challenges caused by MELAS and the unusual occurrence of acute cortical deafness, that to our knowledge has not be described so far in a child in this setting.


Subject(s)
Deafness/etiology , MELAS Syndrome/complications , Child , Hearing Loss, Central/etiology , Humans , Male , Stroke/complications
2.
Neuropediatrics ; 47(1): 61-3, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26569158

ABSTRACT

The assessment of acute vertigo in childhood is often challenging, but fortunately a central cause is rarely identified. We present the case of a 7-year-old boy who developed, after a mild head trauma, a rotary vertigo associated with nausea and vomiting. A posttraumatic peripheral vestibular dysfunction was first suspected but not confirmed by an otoneurological evaluation. When subtle neurological signs were elicited, a brain magnetic resonance imaging was promptly requested. This showed a small infarct on the lateral posterior left part of the medulla oblongata of the brainstem, typical of Wallenberg syndrome. Vascular imaging was normal and no defined etiology was found. The child was started on prophylactic acetylsalicylic acid. The rapid disappearance of vertigo was noted. On follow-up at 6 months, there has been no recurrence and neurological examination was fully normal. Our case extends the differential diagnosis of acute vertigo in childhood that rarely includes the possibility of a brainstem infarct whose recognition through appropriate clinical examination is nevertheless capital for appropriate investigations and management.


Subject(s)
Lateral Medullary Syndrome/complications , Vertigo/diagnosis , Vertigo/etiology , Child , Diffusion Magnetic Resonance Imaging , Humans , Magnetic Resonance Imaging , Male , Medulla Oblongata/pathology
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