The NOTCH gene was identified approximately 110 years ago. Classical studies have
revealed that NOTCH signaling is an evolutionarily conserved pathway. NOTCH receptors …

Degenerative cervical myelopathy (DCM) encompasses various pathological conditions
causing spinal cord (SC) impairment, including spondylosis (multiple level degeneration) …

Clinical Pediatric Neurology, 6th Edition, by Gerald M. Fenichel, MD, offers you highly
practical assistance in diagnosing and managing the primary neurologic disorders of …

Klippel-Feil syndrome is a congenital defect in the formation or segmentation of the cervical
spine. A wide spectrum of associated anomalies may be present. This heterogeneity has …

There are numerous congenital anomalies of the cervical spine. They can be simple and
clinically inconsequential to complex with serious neurologic and structural implications …

Abstract Study Design Cross-sectional study. Objective To determine the prevalence of KFS
in asymptomatic patients in New York State. Summary of Background Data Klippel-Feil …

Skeletal syndromes are among the most common birth defects. Vertebrate skeletogenesis
involves two major cell types: cartilage-forming chondrocytes and bone-forming osteoblasts …

Esophageal Atresia (EA) is a severe developmental defect of the foregut that presents with
or without a Tracheo-Esophageal Fistula (TEF). The prevalence of EA/TEF over time and …

Degenerative cervical myelopathy (DCM), a recently coined term, encompasses a group of
age-related and genetically associated pathologies that affect the cervical spine, including …

Klippel-Feil syndrome (KFS) is a segmentation malformation of the cervical spine; clinically,
it manifests as a short neck with reduced mobility and a low posterior hairline. Several genes …