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10.1007/s00381-020-04794-1 http://scihub22266oqcxt.onion/10.1007/s00381-020-04794-1 32661640!7356125!32661640     free     free     free       Childs+Nerv+Syst 2020 ; 36 (10): 2227-2228 Nephropedia Template TP {{tp|p=32661640|t=2020. Phacomatoses in the pediatric age group |pdf=|usr=}}{{32661640}} gab.com Text Phacomatoses in the pediatric age group JO: Childs Nerv Syst http://www.kidney.de/pget.php?&tw=1&pmid=32661640 #FOAvip The most common phacomatoses in children that need surgical attention are neurofibromatosis 1 and 2, tuberous sclerosis complex, Sturge-Weber disease, Von Hippel-Lindau disease, and neurocutaneous melanocytosis. All are rare and, as genetically determined disorders, all complex multisystem diseases with multiple manifestations outside the CNS. Diagnostics, management recommendations, and surgical care are age-specific and require individualization. The lifelong multidimensional disease burden demands a multidisciplinary and well-coordinated management approach. The consequence of these boundary conditions is that management of children with a phacomatosis is everything else but simple, straight forward, and intuitive. This Special Annual Issue is designed to serve as an up-to-date encyclopedic reference for all aspects of management of phacomatoses in the pediatric age group. Twit Text FOAVip Phacomatoses in the pediatric age group ????Childs Nerv Syst http://www.kidney.de/pget.php?&tw=1&pmid=32661640 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=32661640 #FOAvip English Wikipedia <ref>{{Cite pmid|32661640}}</ref> Phacomatoses in the pediatric age group #MMPMID32661640 Constantini S; Schuhmann MU Childs Nerv Syst 2020[Oct]; 36 (10): 2227-2228 PMID32661640show ga The most common phacomatoses in children that need surgical attention are neurofibromatosis 1 and 2, tuberous sclerosis complex, Sturge-Weber disease, Von Hippel-Lindau disease, and neurocutaneous melanocytosis. All are rare and, as genetically determined disorders, all complex multisystem diseases with multiple manifestations outside the CNS. Diagnostics, management recommendations, and surgical care are age-specific and require individualization. The lifelong multidimensional disease burden demands a multidisciplinary and well-coordinated management approach. The consequence of these boundary conditions is that management of children with a phacomatosis is everything else but simple, straight forward, and intuitive. This Special Annual Issue is designed to serve as an up-to-date encyclopedic reference for all aspects of management of phacomatoses in the pediatric age group. |*Neurocutaneous Syndromes/diagnosis/therapy[MESH] |*Neurofibromatosis 1[MESH] |*Sturge-Weber Syndrome[MESH] |*Tuberous Sclerosis/complications/diagnosis/therapy[MESH] |*von Hippel-Lindau Disease[MESH] |Child[MESH]Phacomatoses in the pediatric age group (epmc).pdf DeepDyve Pubget Overpricing