The Klippel-Feil Syndrome: a Constellation of Deformities
Overview
Authors
Affiliations
The clinical triad, described by Klippel and Feil in 1912 and consisting in a short neck, a low dorsal hairline and restricted neck mobility, is the result of synostosis of several cervical vertebrae, which may or may not be deformed. In recent years, however, even more attention has been given to associated urological, neurological, cardiopulmonary and locomotor deformities, which significantly increase the morbidity. A multidisciplinary approach and treatment are therefore required. We have studied 18 patients and examined 6 additional records. Of these 24 cases, 18 showed associated deformities. In 14 cases surgery was necessary, including cervical fusion for hypermobility in 3 cases, fusion to treat scoliosis in 5 cases, one cervical rib resection and one Sprengel deformity correction. In addition 3 patients needed cardiac surgery and one patient had a ureter reinserted because of vesico-ureteral reflux.
Pepke W, Renkawitz T, Hemmer S Orthopadie (Heidelb). 2024; 53(10):799-804.
PMID: 39117750 PMC: 11427475. DOI: 10.1007/s00132-024-04537-z.
Xu N, Hung K, Gong X, Fan D, Tian Y, Yan M Orphanet J Rare Dis. 2024; 19(1):141.
PMID: 38561822 PMC: 10985996. DOI: 10.1186/s13023-024-03134-9.
Klippel-Feil: A constellation of diagnoses, a contemporary presentation, and recent national trends.
Zhou P, Poorman G, Wang C, Pierce K, Bortz C, Alas H J Craniovertebr Junction Spine. 2019; 10(3):133-138.
PMID: 31772424 PMC: 6868534. DOI: 10.4103/jcvjs.JCVJS_65_19.
"Clinical triad" findings in pediatric Klippel-Feil patients.
Samartzis D, Kalluri P, Herman J, Lubicky J, Shen F Scoliosis Spinal Disord. 2016; 11:15.
PMID: 27355085 PMC: 4922059. DOI: 10.1186/s13013-016-0075-x.
Klippel Feil Syndrome: A Rare Case Report.
Agarwal A, Goel M, Bajpai J, Shukla S, Sachdeva N J Orthop Case Rep. 2016; 4(3):53-5.
PMID: 27298984 PMC: 4719329. DOI: 10.13107/jocr.2250-0685.197.