Splet20. jan. 2024 · Klippel-Feil syndrome is a rare disorder where two or more vertebrae in the neck are fused together from birth. People living with Klippel-Feil syndrome may have a … SpletKlippel-Feil syndrome is a rare bone disorder distinguished by the abnormal fusion of two or more bones in the neck. Children with the disorder may have a short, webbed neck, …
Noonan Syndrome - an overview ScienceDirect Topics
SpletKlippel-Feil Syndrome (KFS) Klippel-Feil syndrome (KFS) is a condition in which you have two or more neck bones (vertebrae) fused together. KFS causes spine abnormalities and can affect many other body areas. Symptoms include short neck, limited neck mobility and low back-of-head hairline. Treatment depends on severity of your symptoms. SpletWhat condition causes a short neck? What is Klippel-Feil syndrome? Klippel-Feil syndrome is a rare bone disorder distinguished by the abnormal fusion of two or more bones in the neck. Children with the disorder may have a short, webbed neck, decreased range of motion in the head and neck area, and/or a low hairline at the back of the head. daeyoo tech. co. ltd. wenzhou
Klippel-Feil Syndrome: Short Neck and Congenital ... - SpineUniverse
Splet08. dec. 2024 · Summary. Klippel-Feil syndrome (KFS) is a rare skeletal disorder characterized by the congenital fusion of two or more vertebrae of the cervical spine within the neck. Some affected individuals may also have an abnormally short neck, restricted movement of the head and neck and a low hairline at the back of the head (posterior … Splet03. dec. 2024 · It is also called short neck deformity, congenital skeletal torticollis or congenital cervical fusion deformity, which refers to the fusion of two or more cervical vertebrae. Mainly manifested as shortening of the cervical spine. Short neck deformity has three clinical characteristics: short and thick neck, low back hairline, and restricted ... Splet17. okt. 2016 · Short neck Conditions with this feature 5p partial monosomy syndrome MedGen UID: 41345 • Concept ID: C0010314 • Disease or Syndrome Cri-du-chat syndrome was first described by Lejeune et al. (1963) as a hereditary congenital syndrome associated with deletion of part of the short arm of chromosome 5. bioappdl.blogspot.com