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the most common genetic disorders seen 1 in 3000 live births. It is a single gene disorder with autosomal dominant trait but up to 50% of the cases arise due to spontaneous mutation.1 Clinical presentation and prognosis is quite different in every case due to variable expression of the neurofibrin I (NF I gene).2,3 It affects neuro-ectodermal, mesenchymal and endodermal originated tissues. The 7 clinical criteria used to diagnose NF1 are: Six or more café-au-lait spots or hyperpigmented macules greater

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Different Uptake Patterns of Tc-99m MDP on Three Phase Bone Scan in a Neurofibromatosis Type I Patient with Multiple Neurofibromas and Neurofibrosarcoma: Case Report