Araştırma Makalesi
Yıl 1990,
Cilt: 43 Sayı: 3, 749 - 756, 30.09.1990
Öz
Bu çalışmada alt ekstremite distal adelelerinde kuvvet kaybı ve çorap tarzında hipoestezi, derin duyu kaybı ile alt ekstremite reflekslerinde azalma tesbit edilen ve histopatolojik tetkiklerle Tip II herediter sensorimotor nöropati teşhisi konan 2 erkek kardeş, elektron mikroskobik bulguları ile birlikte takdim edilmektedir.
Anahtar Kelimeler
Kaynakça
- 1. Dyck PJ : Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurones, In Peripheral Neuropathy, Volume 2. Second edition, Edited by P.J. Dyek, P.K. Thomas, E.H, Lambert and R. Bunge, Philadelphia and London : W.B. Saunders p : 1600.
- 2. Hughes JT Brownell B : Pathology of peroneal muscular atrophy (Charcot-MarieTooth disease), J Neurol Neurosurg Psychiatr 35 : 648, 1972.
- 3. Ludwin SK : Remyelination in the central nervous system and the peripheral nervous system. Adv Neurol 47 : 215, 1987.
- 4. Ouvrier RA MeLeod JG Conchin TE : The hypertrophic forms of hereditary m0otor and sensory neuropatlıy. Brain 110 : 121, 1987.
- 5. Rossi LN Lütschg J Meier C Vasselle F : Hereditary motor sensory neuropathies in childhood. Develop Med Child Newrol 25 ; 19, 1983.
- 6. Ruiz C Rivas F Ramirez-Casillas G Vazguez-Santana R Mendoza-Chalita B Feria Velasco A Tapia-Arizmendi G Cantu JM : A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot Marie-Tooth disease, Clin Genetics 31 : 109, 1987.
- 7. Vogel P Gabriel M Goebel HH Dyck PJ: Hereditary motor sensory neuropakhıy type ll with neurofilament accumulation : New finding or new disorder? Ann Neurol 17 : 455, 1985.
Hereditary Sensory And Mütor Neuropathy - Electron Microscopy A report of twa cases with electron microscopic findings
Öz
İn this paper, we present tWO brothers with distal weakness of lower extremities. They had elsoa marked decrease in pin sensation with a marked diminution in perception of joint position and vibration in a stocking distribution. Electrophysiologic and electron microscopic findings were compatible with hereditary sensory and motor neuropathy (type ID.
Anahtar Kelimeler
Kaynakça
- 1. Dyck PJ : Inherited neuronal degeneration and atrophy affecting peripheral motor, sensory, and autonomic neurones, In Peripheral Neuropathy, Volume 2. Second edition, Edited by P.J. Dyek, P.K. Thomas, E.H, Lambert and R. Bunge, Philadelphia and London : W.B. Saunders p : 1600.
- 2. Hughes JT Brownell B : Pathology of peroneal muscular atrophy (Charcot-MarieTooth disease), J Neurol Neurosurg Psychiatr 35 : 648, 1972.
- 3. Ludwin SK : Remyelination in the central nervous system and the peripheral nervous system. Adv Neurol 47 : 215, 1987.
- 4. Ouvrier RA MeLeod JG Conchin TE : The hypertrophic forms of hereditary m0otor and sensory neuropatlıy. Brain 110 : 121, 1987.
- 5. Rossi LN Lütschg J Meier C Vasselle F : Hereditary motor sensory neuropathies in childhood. Develop Med Child Newrol 25 ; 19, 1983.
- 6. Ruiz C Rivas F Ramirez-Casillas G Vazguez-Santana R Mendoza-Chalita B Feria Velasco A Tapia-Arizmendi G Cantu JM : A distinct congenital motor and sensory neuropathy (neuronal type) with dysmorphic features in a father and two sons. A variant of Charcot Marie-Tooth disease, Clin Genetics 31 : 109, 1987.
- 7. Vogel P Gabriel M Goebel HH Dyck PJ: Hereditary motor sensory neuropakhıy type ll with neurofilament accumulation : New finding or new disorder? Ann Neurol 17 : 455, 1985.
Toplam 7 adet kaynakça vardır.
Ayrıntılar
| Birincil Dil | Türkçe |
|---|---|
| Konular | Histoloji ve Embriyoloji |
| Bölüm | Makaleler |
| Yazarlar | |
| Yayımlanma Tarihi | 30 Eylül 1990 |
| Yayımlandığı Sayı | Yıl 1990 Cilt: 43 Sayı: 3 |
