Add to ORKGNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder with aprevalence of 1 in 2000. About 5% of NF1 patients present with (congenital) bowing of a long bone resulting in pseudarthrosis, usually unilaterally. In most cases the congenital pseudarthrosis (PA) affects the tibia and the pathogenesis of this condition is currently unknown. Diverse treatment options for the NF1-related PA are available. Individuals with NF1 are however susceptible to recurrent fractures and if bridging of the CPA remains elusive or recurrent fractures occur, amputation of the affected limb is oftentimes the only option. To gain more insight into the pathogenesis underlying NF1-related PA, we studied pseudarthrosis cells and periosteum cells of the af...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
The skeleton is frequently affected in individuals with neurofibromatosis type 1, and some of these ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximately 1 in 2,000 ...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
peer reviewedNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximatel...
peer reviewedNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximatel...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
UNLABELLED: A strong relationship between congenital pseudarthrosis of the tibia (CPT) and neurofibr...
Osseous abnormalities, including long-bone dysplasia with pseudarthrosis (PA), are associated with n...
Tibial pseudarthrosis (PA) is a clinically challenging orthopaedic complication that is often associ...
Osseous abnormalities, including long-bone dysplasia with pseudarthrosis (PA), are associated with n...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
The skeleton is frequently affected in individuals with neurofibromatosis type 1, and some of these ...
Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximately 1 in 2,000 ...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
peer reviewedNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximatel...
peer reviewedNeurofibromatosis type 1 (NF1) is an autosomal dominant disorder affecting approximatel...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
UNLABELLED: A strong relationship between congenital pseudarthrosis of the tibia (CPT) and neurofibr...
Osseous abnormalities, including long-bone dysplasia with pseudarthrosis (PA), are associated with n...
Tibial pseudarthrosis (PA) is a clinically challenging orthopaedic complication that is often associ...
Osseous abnormalities, including long-bone dysplasia with pseudarthrosis (PA), are associated with n...
Congenital pseudarthrosis of the tibia (CPT) is a rare disease which normally presents itself during...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
Neurofibromatosis type 1 (NF1) is a prevalent genetic disorder primarily characterized by the format...
The skeleton is frequently affected in individuals with neurofibromatosis type 1, and some of these ...