Look up: Klippel Feil Syndrome

1. Klippel Feil Syndrome
   A rare birth disorder that affects the cervical vertebrae. As the fetus is forming and developing during pregnancy, the vertebrae in the neck do not divide properly and will become fused together. Common signs of the disorder include a short neck, low hairline and decreased movement abilities in the...
   Found on http://www.pregnology.com/AZ/K/1
   
   
2. Klippel-Feil syndrome
   Klippel-Feil syndrome: See: Klippel-Feil sequence.Common Misspellings: klippel-feil syndrone
   Found on http://www.medterms.com/script/main/art.
   
   
3. klippel-feil syndrome
   <syndrome> Fused vertebrae, especially cervical spine (C3-C4), elevation of scapula (Sprengel deformity), omocervical bones, GU abnormalities (66%), renal agenesis (33%), deafness (33%) ... (12 Dec 1998) ...
   Found on http://www.mondofacto.com/facts/dictiona
   
   
4. Klippel-Feil syndrome
   (klĭ-pel´ fīl´) shortness of the neck due to reduction in the number of cervical vertebrae or the fusion of multiple hemivertebrae into one osseous mass, with limitation of neck motion and low hairline.
   Found on http://www.encyclo.co.uk/local/21001
   
   
5. Klippel-Feil syndrome
   Type: Term Pronunciation: klip′ĕl fīl Definitions: 1. a congenital defect manifested as a short neck, fusion of cervical vertebrae, and abnormalities of the brainstem and cerebellum; autosomal dominant inheritance, with most cases sporadic. Synonyms: cervical fusion syndrome
   Found on http://www.medilexicon.com/medicaldictio
   
   
6. Klippel–Feil syndrome
   | ICD9 = | ICDO = | OMIM = 118100 | OMIM_mult = | MedlinePlus = | eMedicineSubj = orthoped | eMedicineTopic = 408 | MeshID = D007714 | --> `Klippel–Feil syndrome` is a rare disease, initially reported in 1912 by Maurice Klippel and André Feil from France, characterized by the congenital...
   Found on http://en.wikipedia.org/wiki/Klippelââ‚