Research Article
Year 1990,
Volume: 43 Issue: 3, 749 - 756, 30.09.1990
Abstract
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.
References
- 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
Abstract
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.
References
- 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.
There are 7 citations in total.
Details
| Primary Language | Turkish |
|---|---|
| Subjects | Histology and Embryology |
| Journal Section | Articles |
| Authors | |
| Publication Date | September 30, 1990 |
| Published in Issue | Year 1990 Volume: 43 Issue: 3 |
