Searchable abstracts of presentations at key conferences on calcified tissues

ba0007p125 | (1) | ICCBH2019

SCN8a mutations and osteoporosis. Is osteocyte dysfunction the cause or the consequence?

O'Donnell Gillian , Halpenny Leah , Burke Eleanor , McCarron Laura , Sheridan Sabrina , McDonnell Ciara

Background: Mutations in the SCN8a gene, which encodes one of the most abundant voltage gated sodium channels; Nav1.6, has a strong association with epileptic encephalopathy type 13, ataxia, muscle atrophy and intellectual disability. Previous cases of pathological skeletal fractures in children with known SCN8a mutations have been published but the source of the related skeletal mechanism remains unclear.Presenting problem: The proband presented at 15mo...