2020, Number 2
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Acta Med 2020; 18 (2)
C2-C3 cervical synostosis: Klippel-Feil syndrome
Domínguez CLG, Colín GCG, Reyes VE
Language: Spanish
References: 4
Page: 214-215
PDF size: 138.89 Kb.
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REFERENCES
Karaca E, Yuregir OO, Bozdogan ST, Aslan H, Pehlivan D, Jhangiani SN et al. Rare variants in the notch signaling pathway describe a novel type of autosomal recessive Klippel-Feil syndrome. Am J Med Genet A. 2015; 167A: 2795-2799.
Samartzis D, Kalluri P, Herman J, Lubicky JP et al. “Clinical triad” findings in pediatric Klippel-Feil patients. Scoliosis Spinal Disord. 2016; 11: 15-16.
Kenna MA, Irace AL, Strychowsky JE, Kawai K et al. Otolaryngologic manifestations of Klippel-Feil syndrome in children. JAMA Otolaryngol Head Neck Surg. 2018; 144: 238-243.
Gruber J, Saleh A, Bakhsh W, Rubery PT et al. The prevalence of Klippel-Feil syndrome: a computed tomography-based analysis of 2,917 patients. Spine Deform. 2018; 6: 448-453.
Full text
10.35366/93903