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Genetic Conditions Affecting the Skeleton : Congenital, Idiopathic Scoliosis and Arthrogryposis



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Autore: Giampietro Philip Visualizza persona
Titolo: Genetic Conditions Affecting the Skeleton : Congenital, Idiopathic Scoliosis and Arthrogryposis Visualizza cluster
Pubblicazione: Basel, : MDPI - Multidisciplinary Digital Publishing Institute, 2022
Descrizione fisica: 1 electronic resource (172 p.)
Soggetto topico: Research & information: general
Biology, life sciences
Genetics (non-medical)
Soggetto non controllato: spinal curvatures
scoliosis
idiopathic
DNA methylation
pyrosequencing
estrogen receptor 1
ESR1
scoliosis progression
adolescent idiopathic scoliosis
idiopathic scoliosis
exome sequencing
spine
polygenic
variants
musculoskeletal disease
cytoskeleton
extracellular matrix
contracture
arthrogryposis
congenital
POC5
cilia
genetics
spine deformity
genetic predisposition
complex trait
model animal
genome wide association study
genetic linkage study
Amyoplasia
DECIPHER (DatabasE of genomiC variation and Phenotype in Humans using Ensemble Resources)
CNV (copy number variant)
DA (distal arthrogryposis)
IPA (ingenuity pathway analysis)
HPO (human phenotype ontology)
akinesia
MYOD
IGF2
FGFR1 (Fibroblast growth factor receptor 1)
genetic variations
congenital scoliosis
monozygotic twin
epigenome-wide association study
bone
discordant
curve severity
differentially methylated region
congenital vertebral malformation
copy number variant
CNV
CHRNG
distal arthrogryposis type 8
Escobar
multiple pterygium syndrome
MYH3
protein tyrosine kinase 7 (PTK7)
whole exome sequencing
Persona (resp. second.): Hadley-MillerNancy
RaggioCathy L
GiampietroPhilip
Sommario/riassunto: In this Special Issue of Genes entitled “Genetic Conditions Affecting the Skeleton: Congenital, Idiopathic Scoliosis and Arthrogryposis”, evidence is presented that suggests that congenital, idiopathic scoliosis, and arthrogryposis share similar overlapping, but also distinct, etiopathogenic mechanisms, including connective tissue and neuromuscular mechanisms. Congenital scoliosis (CS) is defined by the presence of an abnormal spinal curvature, due to an underlying vertebral bony malformation (VM). Idiopathic scoliosis (IS) is defined by the presence of an abnormal structural spinal curvature of ≥10 degrees in the sagittal plane, in the absence of an underlying VM. Arthrogryposis is defined by the presence of congenital contractures in two or more joints of the appendicular skeleton. All three conditions have complex genetic causes. This Special Issue highlights the complex nature of these conditions and current concepts in our approach to better understand their genetics.
Altri titoli varianti: Genetic Conditions Affecting the Skeleton
Titolo autorizzato: Genetic Conditions Affecting the Skeleton  Visualizza cluster
ISBN: 3-0365-5976-0
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910639995403321
Lo trovi qui: Univ. Federico II
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