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.
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MadaanPMukherjeeSReddyC, et al.Multiple café-au-lait macules and movement disorder: think beyond neurofibromatosis. Arch Dis Child2021; 106: 73–73.
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MadaanPSinganamallaBSainiL. Conventional teaching: classical clues. Indian J Pediatr2021; 88: 196–197.
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