Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

Neurofibromatosis type 1

Neurofibromatosis type 1 (NF1) is a clinically heterogeneous, neurocutaneous genetic disorder characterized by café-au-lait spots, iris Lisch nodules, axillary and inguinal freckling, and multiple neurofibromas.

Tetraparesis

Weakness of all four limbs.

Total: 2

(per page)

PMID (PMCID)
24436700 (3699244)	OTHER
	Vascularized fibula strut graft used in neurofibromatosis type 1-related kyphosis: a case of almost complete reversal of deformity-induced tetraparesis.
	Melloh M, Hodgson B, Carstens A, Cornwall J. Evid Based Spine Care J. 2013;4(1):59-62.
	Conclusions8195This case report demonstrates the existence of a potential local option for the difficult problems of pseudoarthrosis, progressive spinal deformity, and cord compromise in patients with neurofibromatosis type 1-related kyphosis resulting in an almost complete reversal of deformity-induced tetraparesis.
24436700 (3699244)	OTHER
	Vascularized fibula strut graft used in neurofibromatosis type 1-related kyphosis: a case of almost complete reversal of deformity-induced tetraparesis.
	Melloh M, Hodgson B, Carstens A, Cornwall J. Evid Based Spine Care J. 2013;4(1):59-62.
	Vascularized fibula strut graft used in neurofibromatosis type 1-related kyphosis: a case of almost complete reversal of deformity-induced tetraparesis.