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Trop Doct ; 51(4): 604-605, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34167384

ABSTRACT

Neurofibromatoses are inherited tumour-suppressive disorders that are characterised by multiple neoplastic and non-neoplastic tumours. Neurofibromatosis type 1 is a common disorder with multiple neurofibromas with widespread complications. We here report a seven-year old boy presenting with first episode of seizure and multiple café-au-lait macules but neuroimaging revealed corpus callosal changes without any focal areas of signal intensities.


Subject(s)
Neurofibromatoses , Neurofibromatosis 1 , Cafe-au-Lait Spots , Child , Corpus Callosum/diagnostic imaging , Humans , Male , Neurofibromatosis 1/diagnosis , Neuroimaging
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