TY  - JOUR
AU  - Vujasinović-Stupar, Nada
AU  - Pavlov-Dolijanović, Slavica
AU  - Hatib, Nur
AU  - Banko, Bojan
AU  - Đukić, Milan
AU  - Nikolić-Jakoba, Nataša
PY  - 2016
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/2142
AB  - Klippel-Feil syndrome is defined as congenital fusion of two or more cervical vertebrae. In this article, we report a 55-year-old male patient with one-year history of neck pain, headaches, and one episode of syncope after a severe trauma. X-rays and magnetic resonance imaging of cervical spine revealed fused vertebral bodies of C2-C5. The major anomalies associated with Klippel-Feil syndrome (small stature, thoracic kyphoscoliosis, lumbar scoliosis, restricted opening mouth, and bilateral sensorineural hearing loss) as well as multiple minor anomalies (mild face asymmetry, high arched palate, rhinoscoliosis, high nasal bridge, inclined septi nasi, and thin upper lip) were detected. This is a rare case describing the anomalies of the nose in Klippel-Feil syndrome patients. Our patient had no central cord impairment following a severe trauma.
PB  - Turkish League Against Rheumatism, Ankara
T2  - Archives of Rheumatology
T1  - Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report
VL  - 31
IS  - 1
SP  - 82
EP  - 86
DO  - 10.5606/ArchRheumatol.2016.5714
ER  - 

@article{
author = "Vujasinović-Stupar, Nada and Pavlov-Dolijanović, Slavica and Hatib, Nur and Banko, Bojan and Đukić, Milan and Nikolić-Jakoba, Nataša",
year = "2016",
abstract = "Klippel-Feil syndrome is defined as congenital fusion of two or more cervical vertebrae. In this article, we report a 55-year-old male patient with one-year history of neck pain, headaches, and one episode of syncope after a severe trauma. X-rays and magnetic resonance imaging of cervical spine revealed fused vertebral bodies of C2-C5. The major anomalies associated with Klippel-Feil syndrome (small stature, thoracic kyphoscoliosis, lumbar scoliosis, restricted opening mouth, and bilateral sensorineural hearing loss) as well as multiple minor anomalies (mild face asymmetry, high arched palate, rhinoscoliosis, high nasal bridge, inclined septi nasi, and thin upper lip) were detected. This is a rare case describing the anomalies of the nose in Klippel-Feil syndrome patients. Our patient had no central cord impairment following a severe trauma.",
publisher = "Turkish League Against Rheumatism, Ankara",
journal = "Archives of Rheumatology",
title = "Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report",
volume = "31",
number = "1",
pages = "82-86",
doi = "10.5606/ArchRheumatol.2016.5714"
}

Vujasinović-Stupar, N., Pavlov-Dolijanović, S., Hatib, N., Banko, B., Đukić, M.,& Nikolić-Jakoba, N.. (2016). Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report. in Archives of Rheumatology
Turkish League Against Rheumatism, Ankara., 31(1), 82-86.
https://doi.org/10.5606/ArchRheumatol.2016.5714

Vujasinović-Stupar N, Pavlov-Dolijanović S, Hatib N, Banko B, Đukić M, Nikolić-Jakoba N. Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report. in Archives of Rheumatology. 2016;31(1):82-86.
doi:10.5606/ArchRheumatol.2016.5714 .

Vujasinović-Stupar, Nada, Pavlov-Dolijanović, Slavica, Hatib, Nur, Banko, Bojan, Đukić, Milan, Nikolić-Jakoba, Nataša, "Multiple Major and Minor Anomalies Associated With Klippel-Feil Syndrome: A Case Report" in Archives of Rheumatology, 31, no. 1 (2016):82-86,
https://doi.org/10.5606/ArchRheumatol.2016.5714 . .