WebDec 20, 2011 · Several lines of evidence indicate that the pathogenic mechanism underlying the autosomal dominant spectrum of disorders due to mutations in FLNB that ... is similar to that operating to cause the FLNA- and FLNB-related disorders. Outside the filamin gene family, a similar mechanism has been invoked for gain-of-function mutations in ... WebNM_001457.4(FLNB):c.6956T>C (p.Ile2319Thr) AND FLNB-Related Spectrum Disorders Clinical significance: Likely benign (Last evaluated: Jan 13, 2024) Review status: 1 star …
FLNB Disorders - GeneReviews® - NCBI Bookshelf
WebApr 5, 2024 · The location and/or type of variants in FLNB result in a spectrum of osteochondrodysplasias ranging from mild forms, like spondylocarpotarsal synostosis syndrome and Larsen syndrome, to severe ... WebApr 11, 2024 · Autism is a neurodevelopmental disorder of the brain function that affects the person’s speech, communication, interaction, learning, and behavior. It is a complex disease with diverse etiology and multiple factors. They are neurodevelopmental disorders because it generally occurs in the first two years of life. rapina agrate
Variants in gene FLNB - ClinVar Miner
WebList of variants in gene FLNB studied for FLNB-Related Spectrum Disorders Minimum submission review status: Collection method: Minimum conflict level: Report conflict between different conditions Gene type ... WebNM_001457.4(FLNB):c.6017A>G (p.Lys2006Arg) AND FLNB-Related Spectrum Disorders Clinical significance: Likely benign (Last evaluated: Jan 13, 2024) Review status: 1 star out of maximum of 4 stars WebJan 6, 2024 · Background Loss of function or gain of function variants of Filamin B (FLNB) cause recessive or dominant skeletal disorders respectively. Spondylocarpotarsal synostosis syndrome (SCT) is a rare autosomal recessive disorder characterized by short stature, fused vertebrae and fusion of carpal and tarsal bones. We present a novel FLNB … rapina aggravata