Klippel-FeilSyndromewithSprengelDeformitySprengel畸形的Klippel-Feil综合征 系统标签: sprengelklippelfeildeformitysyndrome综合征 RadiologyCase.2019May;13(5):24-29PediatricRadiology:Klippel-FeilSyndromewithSprengelDeformityGeorgievetal.JournalofRadiologyCaseReportswww.RadiologyCases.com24Klippel-FeilSyndromewithSprengelDefo...
Klippel-Feil syndrome (KFS) classically describes the patient with fused cervical vertebrae and the clinical triad of a short neck, low posterior hairline, and decreased range of motion of the neck. Although this constellation of attributes was originally recognized in 1912 (31,32), identification ...
This case is the first report of a Chiari type zero in association with Klippel-Feil syndrome (KFS). There is a paucity of literature surrounding the management of Chiari malformations in the setting of acute spinal cord injury. Case description An 18 year old male was transferred to our inst...
Dandy-WalkerCephaloceleCraniovertebral junctionScoliosisOmovertebral boneBackground Klippel-Feil syndrome (KFS) is a congenital malformation causing fusion of at least two cervical vertebrae and characterized clinically by presence of triad of short neck, limited neck movements, and low posterior hair ...
Klippel-Feil syndrome is defined as congenital fusion of two or more cervical vertebrae and is believed to result from faulty segmentation along the embryo's developing axis during weeks 3–8 of gestation. Persons with Klippel-Feil syndrome and cervical stenosis may be at increased risk for spinal...
Klippel-Feil syndrome (KFS) is characterised by congenital vertebral fusion of the cervical spine and a wide spectrum of associated anomalies... RA Clarke,G Catalan,AD Diwan,... - 《Pediatric Radiology》 被引量: 161发表: 1998年 Interleukin-6 in serum of patients with polymyalgia rheumatica and...
Of fifty patients with the diagnosis of Klippel-Feil syndrome, less than half had the classic clinical triad of findings, while more than half had scoliosis, and a third had renal anomalies. All patients were at risk of having other serious, but less apparent, anomalies, including: Sprengel'...
Background Klippel-Feil syndrome (KFS) is characterized by specific congenital anomalies of segmentation of the cervical spine. On the other hand, dermoid tumour is a rare entity accounting for 0.04–0.7% of all intracranial tumours and the most common location is in the posterior fossa, ...
Heterogeneity in Klippel-Feil syndrome: a new classifi- cation. Pediatr Radiol 1998;28:967-74.Clarke RA, Catalan G, Diwan AD. Heterogeneity in Klip- pel-Feil syndrome: a new classification. Pediatr Radiology. 1998; 28: 967-74.Clarke RA, Cat alan G, Diwan AD, Kearsley JH. Hetero- gene...
Klippel-Feil Syndrome2023 by Razi Vaccine & Serum Research Institute.Klippel-Feil Syndrome (KFS) is a rare genetic disorder characterized by the abnormal development of the cervical spine, leading to the fusion of two or more cervical vertebrae. The syndrome presents diverse symptoms, including ...