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Arch Pediatr ; 16(5): 444-8, 2009 May.
Article in French | MEDLINE | ID: mdl-19339164

ABSTRACT

Fahr syndrome is defined by the presence of striopallidal notched bilateral and symmetric calcifications at the base of the skull. We report an observation of a 12-year-old girl who presented gait impairment, seizures, somnolence and aphasia. Brain computed tomodensitometry identified intracranial calcifications. The tests demonstrated pseudohypoparathyroidism.


Subject(s)
Basal Ganglia Diseases/diagnosis , Calcinosis/diagnosis , Pseudohypoparathyroidism/etiology , Aphasia/etiology , Basal Ganglia Diseases/diagnostic imaging , Brain/diagnostic imaging , Calcinosis/diagnostic imaging , Child , Female , Gait Apraxia/etiology , Humans , Syndrome , Tomography, X-Ray Computed
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