Sindroma Klippel-Feil : Suatu Tinjauan Neuroanatomi  

Oleh:

Sasmita, Poppy Kristina

Jenis: Article from Journal - ilmiah nasional - tidak terakreditasi DIKTI
Dalam koleksi: Widya: Majalah Ilmiah vol. 18 no. 190 (Jul. 2001), page 43.
Topik: sindroma klippel-feil; tinjauan neuroanatomi

Ketersediaan

Perpustakaan Pusat (Semanggi) Nomor Panggil: MM47.17 Non-tandon: 1 (dapat dipinjam: 0) Tandon: tidak ada

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Isi artikel

Klipper-feil syndrome describes congenital fusion of at least two of the seven vertebrae in the spine. There may be fusion or anomalies of vertebrae in the thoracic or lumbal spine. Many people actually have the syndrome but are never diagnosed because their symptoms may be so minimal. Shortness of the neck, low psoterior hair line and limited movement of the neck, are the most common features of the syndrome. For symptomatic patients with mechanical problems, the usual treatment measures for degenerative osteoarthritis are applicable and include traction, a cervical collar and analgetics. With clinical evidence for compression of the cervival cord, laminectomy is indicated.

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