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Quoted phrase not found in phrase index: "Abnormality of the posterior hairline"
Page 1
Bilateral Multilevel Cervical Rib and Bilateral Omovertebra in Klippel-Feil Syndrome.
Satış S, Alparslan N, Tuna M, Dere O, Yetişgin A. Satış S, et al. World Neurosurg. 2020 Apr;136:62-65. doi: 10.1016/j.wneu.2020.01.010. Epub 2020 Jan 10. World Neurosurg. 2020. PMID: 31931249
BACKGROUND: Klippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical joint range of motion are the classical triad of this disease. In this syndrome, which is rarely observed, the characteristics that hav …
BACKGROUND: Klippel-Feil syndrome was first described in 1912; a short neck, low posterior hairline, and decreased cervical jo …
The value of a simple method to decrease diagnostic errors in Turner syndrome: a case report.
Mousavi S, Amiri B, Beigi S, Farzaneh M. Mousavi S, et al. J Med Case Rep. 2021 Feb 18;15(1):79. doi: 10.1186/s13256-021-02673-0. J Med Case Rep. 2021. PMID: 33596986 Free PMC article.
Therefore, a more thorough physical examination was performed, in which high arched palate and low posterior hairline were observed. There was also a difference between target height and patient height standard deviation scores. ...This case report int …
Therefore, a more thorough physical examination was performed, in which high arched palate and low posterior hairline were …
Brief clinical report: duplication of distal 17q: report of an observation.
Naccache NF, Vianna-Morgante AM, Richieri-Costa A. Naccache NF, et al. Am J Med Genet. 1984 Mar;17(3):633-9. doi: 10.1002/ajmg.1320170313. Am J Med Genet. 1984. PMID: 6711615
Anomalies present in greater than or equal to 75% of the patients were severe psychomotor retardation; short stature; microcephaly; frontal bossing and temporal retraction; widow's peak; narrow palpebral fissures; flat nasal bridge; thin upper lip overlapping thin lower lip; down …
Anomalies present in greater than or equal to 75% of the patients were severe psychomotor retardation; short stature; microcephaly; frontal …
Mutations in MEOX1, encoding mesenchyme homeobox 1, cause Klippel-Feil anomaly.
Mohamed JY, Faqeih E, Alsiddiky A, Alshammari MJ, Ibrahim NA, Alkuraya FS. Mohamed JY, et al. Am J Hum Genet. 2013 Jan 10;92(1):157-61. doi: 10.1016/j.ajhg.2012.11.016. Epub 2013 Jan 3. Am J Hum Genet. 2013. PMID: 23290072 Free PMC article.
Klippel-Feil syndrome (KFS) is a segmentation malformation of the cervical spine; clinically, it manifests as a short neck with reduced mobility and a low posterior hairline. Several genes have been proposed as candidates for KFS when it is present with other associ …
Klippel-Feil syndrome (KFS) is a segmentation malformation of the cervical spine; clinically, it manifests as a short neck with reduced mobi …
Repeated anesthetic management for a patient with Klippel-Feil syndrome.
Hase Y, Kamekura N, Fujisawa T, Fukushima K. Hase Y, et al. Anesth Prog. 2014 Fall;61(3):103-6. doi: 10.2344/0003-3006-61.3.103. Anesth Prog. 2014. PMID: 25191983 Free PMC article.
Klippel-Feil syndrome (KFS) is a rare disease characterized by a classic triad comprising a short neck, a low posterior hairline, and restricted motion of the neck due to fused cervical vertebrae. ...The patient had an extremely small mandible, significant retrognat …
Klippel-Feil syndrome (KFS) is a rare disease characterized by a classic triad comprising a short neck, a low posterior hairline …
The Klippel-Feil syndrome: a case report.
Lagravère MO, Barriga MI, Valdizán C, Saldarriaga A, Pardo JF, Flores M. Lagravère MO, et al. J Can Dent Assoc. 2004 Nov;70(10):685-8. J Can Dent Assoc. 2004. PMID: 15530267 Free article.
Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy with a short neck, low-set posterior hairline, deafness and limited neck motion was suspected of having such a condition. ...
Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy …