how to cite this article: karimzadeh p, jafari n, nejad biglari hb, jabbehdari s, alizadeh m, alizadeh gh, nejad biglari hm, sanii s. the clinical features and diagnosis of adrenoleukodystrophy: a case series of iranian family. iran j child neurol. winter 2016; 10(1):61-64. abstract objective adrenoleukodystrophy disorder is one of the x-linked genetic disorders caused by the myelin sheath brea...

two iranian families with autosomal dominant dementia-plus were observed. one family includes 3 affected members and the other includes 4. the two families showed a dominantly inherited complex neurological syndrome with onset in childhood to adulthood. one patient showed prominent anticipation of the onset age. onset was with cerebellar signs followed by dementia, seizures, and extrapyramidal ...

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