Leger gjør feil
نویسندگان
چکیده
منابع مشابه
Klippel Feil syndrome
In 1912, Klippel and Feil (1) first reported on a patient with a short neck, a low posterior hairline, and severe restriction of neck movements due to complete fusion of the cervical spine, the classic clinical triad which is the hallmark of Klippel-Feil syndrome (KFS). It is estimated to occur in 1 in 40,000 to 42,000 newborns worldwide. Mutations in the GDF6 and GDF3 genes can cause KFS (2). ...
متن کاملAutosomal recessive Klippel-Feil syndrome.
In 1912, Klippel and Feill reported the first clinical details and necropsy findings of a syndrome characterised by the triad short or absent neck, severe limitation of head movement, and low posterior hairline. An Egyptian mummy (from 500 BC) is the oldest subject in whom Klippel-Feil syndrome has been seen.2 Another interesting observation is the similarity between the figure of an old man de...
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We reviewed the outcome of 53 primary St. Leger total knee replacement (TKR) implanted into 47 patients over a 2-year period from March 1995 and compared the outcome with age and sex matched controls with the Kinemax Plus TKR. All operations were performed to treat osteoarthritis of the knee. The St. Leger replacements were done in a Teaching Hospital by a Consultant surgeon while the Kinemax P...
متن کاملKlippel-Feil Syndrome and Unilateral Diaphragmatic Paralysis
Figure 1. Sagittal plane, T2-weighted sequence with contrast showing segmentation anomalies of cervical vertebrae.
متن کاملThe Klippel-Feil syndrome: a case report.
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. Clinical and radiographic examination led to the diagnosis of Klippel-Feil syndrome.
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ژورنال
عنوان ژورنال: Tidsskrift for Den norske legeforening
سال: 2018
ISSN: 0029-2001
DOI: 10.4045/tidsskr.18.0210