One Case of Klippel-Fiel Syndrome
نویسندگان
چکیده مقاله:
A case of Klippel-Feil disease with epilepsy is reported and the clinical, X-ray, EE G changes in this patient are discussed and compared with the findings in the other reports. The treatment is symptomatic.
منابع مشابه
[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.
متن کامل[A case of Klippel-Trenaunay syndrome].
The case of a 33-year-old woman suffering from the Klippel-Trenaunay-syndrome which belongs to the syndromes of dysplasia is discussed. The cases in question is an anaeviformous variant. Apart from this there exists a renal hypoplasia which is to be seen within the Klippel-Trenaunay-syndrome. This renal hypoplasia has led to a terminal renal insufficiency and has made necessary a chronic haemod...
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 کاملKlippel - Trenaunay - Weber syndrome — a case report
syndrome is a rare congenital syndrome involving enlarged veins and arteries, limb hypertrophy and capillary malformations. In 1900, French physicians, Klippel and Trenaunay, first described what became known as Klippel-Trenaunay syndrome after two patients presented with a triad of symptoms — port-wine stain, varicose veins, and bony and soft tissue hypertrophy involving an extremity (Klippel ...
متن کاملKlippel Trenaunay Syndrome: A Case Report.
Klippel Trenaunay syndrome refers to a rare congenital anomaly which is characterized by capillary malformation, venous malformation and sometimes lymphatic malformation associated with overgrowth of a limb, with soft tissue hypertrophy and/or bony hypertrophy. The anomaly, if present, is present at birth and usually involves the lower limbs as well as portion of trunk, face, uppper limb or hea...
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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عنوان ژورنال
دوره 2 شماره 4
صفحات 283- 288
تاریخ انتشار 1974-04
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