Larsen Sendromu: Yenidoğan Döneminde Literatür Eşliğinde Bir Olgu Sunumu
Abstract
Keywords
References
- Bicknell LS, Farrington-Rock C, Shafeghati Y, et al. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB. Journal of Medical Genetics 2006;44(2):89–98.
- Harris R, Cullen CH. Autosomal dominant inheritance in Larsen’s syndrome. Clin Genet 1971;2:87-90.
- Steel HH, Kohl EJ. Multiple congenital dislocations associated with other skeletal anomalies (Larsen syndrome) in three siblings. Am J Bone Jt Surg 1972;54(1):75-81.
- Krakow D, Robertson SP, King LM, et al. Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis. Nature Genet 2004;36:405-10.
- Larsen LJ, Schottstaedt ER, Bost FC. Multiple congenital dislocations associated with characteristic facial abnormality. J. Pediat 1950;37(4):574-81.
- Latta RJ, Graham CB, Aase JM, et al. Larsen's syndrome: a skeletal dysplasia with multiple joint dislocations and unusual facies. J Pediatr 1971;78(2):291-8.
- Kaya R, Türkmenoğlu O, Çavuşoğlu H, et al. Cervical Pedicle Screw Fixation in a Patient with Larsen Syndrome: A Case Report. Turkish Neurosurgery 2006;16(1):48-52.
- Campbell RM. Spine Deformities in Rare Congenital Syndromes. Spine 2009;34(17):1815-27.
Details
Primary Language
Turkish
Subjects
-
Journal Section
-
Authors
Sarman H
This is me
Publication Date
December 1, 2013
Submission Date
August 10, 2015
Acceptance Date
-
Published in Issue
Year 2013 Volume: 5 Number: 3


