A Case of Obstetrical Brachial Plexus Injury Associated with Klippel-Feil Syndrome
نویسندگان
چکیده
منابع مشابه
Klippel-Feil syndrome associated with aortic coarctation.
Aortic coarctation was diagnosed in a 27-year-old man with Klippel-Feil syndrome, an inborn skeletal defect of the vertebral column associated with anomalies of various organs. The presented findings are discussed in the context to the theory of vascular artery supply disruption sequence during embryogenisis as a potential explanation for the pathogenesis of morphological defects of Klippel-Fei...
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.
متن کاملGenitourinary anomalies associated with Klippel-Feil syndrome.
Of thirty-nine patients with Klippel-Feil syndrome, twenty-five (64 per cent) had significant genitourinary-tract anomalies demonstrated by intravenous urogram and physical examination. The incidence of these anomalies in Feil's three types of the syndrome was essentially the same, unilateral renal agenesis being the most common. A routine intravenous urogram is indicated in patients with this ...
متن کاملKlippel-Feil syndrome: a case report.
OBJECTIVE To report the clinical presentation and peculiarity of management of Klippel-Feil syndrome (KFS) at the University of Abuja Teaching Hospital, Gwagwalada. BACKGROUND KFS is a rare pathology that has not been previously reported on in Nigeria. METHODS Case review was employed to report this pathology. RESULT This case is a 10 year old boy with KFS presenting with cosmetic blemish...
متن کامل[A case of Klippel-Feil syndrome].
We would like to present a case of Klippel-Feil Syndrome in which it is associated with multiple cervical vertebra synostosis, short neck, cervical rib, congenital sclerosis, platybasia, spina-bifida and deafness. We are revising the case history of this syndrome.
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ژورنال
عنوان ژورنال: Kafkas Journal of Medical Sciences
سال: 2018
ISSN: 1307-4504
DOI: 10.5505/kjms.2018.38247