2023
DOI: 10.1111/exd.14996
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The role of scoliosis on the comorbidity and demographics of neurofibromatosis type 1 patients: A retrospective analysis of the National Inpatient Sample database

Nilesh Kodali,
Keshav D. Kumar,
Robert A. Schwartz

Abstract: Neurofibromatosis type 1 (NF1) is the most common neurocutaneous syndrome in the United States, affecting every 1 in 3000 individuals. NF1 occurs due to non‐functional mutations in the NF1 gene, which expresses neurofibromin, a protein involved in tumour suppression. As a result, NF1 typically presents with non‐cancerous neoplasm masses called neurofibromas across the body. Out of all NF1 abnormalities, the most common skeletal abnormality seen in around 10%–30% of NF1 patients is scoliosis, an improver curvat… Show more

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“…It is inherited in an autosomal dominant manner and has an incidence of 1 in every 3000 individuals. 1 , 2 Spinal deformity is the most common musculoskeletal manifestation of NF‐1 and is divided into dystrophic and non‐dystrophic types. Dystrophic spinal deformities are associated with neurofibromas, characterized by direct influence of neurofibromas on the structure of the spine, resulting in bone destruction and spinal instability.…”
Section: Introductionmentioning
confidence: 99%
“…It is inherited in an autosomal dominant manner and has an incidence of 1 in every 3000 individuals. 1 , 2 Spinal deformity is the most common musculoskeletal manifestation of NF‐1 and is divided into dystrophic and non‐dystrophic types. Dystrophic spinal deformities are associated with neurofibromas, characterized by direct influence of neurofibromas on the structure of the spine, resulting in bone destruction and spinal instability.…”
Section: Introductionmentioning
confidence: 99%