peripheral tooth

См. также в других словарях:

• Peripheral myelin protein 22 — Peripheral myelin protein 22, also known as PMP22, is a human gene.The integral membrane protein encoded by this gene is a hydrophobic, tetraspan glycoprotein expressed mainly in Schwann cells and is a major component of compact myelin in the… …   Wikipedia

• Peripheral neuropathy — Neuropathy redirects here. For other uses, see Neuropathy (disambiguation). Not to be confused with Nephropathy. Peripheral neuropathy Classification and external resources …   Wikipedia

• Tooth development — Radiograph of lower right (from left to right) third, second, and first molars in different stages of development. Tooth development or odontogenesis is the complex process by which teeth form from embryonic cells, grow, and erupt into the mouth …   Wikipedia

• Peripheral neuropathy — A problem with the functioning of the nerves outside the spinal cord. Symptoms may include numbness, weakness, burning pain * * * peripheral neuropathy n a disease or degenerative state (as polyneuropathy) of the peripheral nerves in which motor …   Medical dictionary

• peripheral neuropathy — polyneuropathy; = peripheral neuritis any of a group of disorders affecting the sensory and/or motor nerves in the peripheral nervous system. They tend to start distally, in the fingers and toes, and progress proximally. Symptoms include pins and …   The new mediacal dictionary

• Charcot–Marie–Tooth disease — Charcot Marie Tooth disease Classification and external resources The foot of a person with Charcot Marie Tooth. The lack of muscle, a high arch, and claw toes are signs of the genetic disease. ICD 10 …   Wikipedia

• Charcot-Marie-Tooth disease — A neuromuscular disease, the most common inherited disorder of peripheral nerves, characterized by progressively debilitating weakness. The disease is also called peroneal muscular atrophy and hereditary motor and sensory neuropathy. The foremost …   Medical dictionary

• Maladie De Charcot-Marie-Tooth Type 1 — La maladie de Charcot Marie Tooth type 1 est la plus fréquente des neuropathies héréditaires du groupe des maladies de Charcot Marie Tooth (environ 50% des cas). C est une maladie dont la transmission génétique est autosomique dominante, et qui… …   Wikipédia en Français

• Maladie de charcot-marie-tooth type 1 — La maladie de Charcot Marie Tooth type 1 est la plus fréquente des neuropathies héréditaires du groupe des maladies de Charcot Marie Tooth (environ 50% des cas). C est une maladie dont la transmission génétique est autosomique dominante, et qui… …   Wikipédia en Français

• Maladie de Charcot-Marie-Tooth type 1 — La maladie de Charcot Marie Tooth type 1 est la plus fréquente des neuropathies héréditaires du groupe des maladies de Charcot Marie Tooth (environ 50% des cas). C est une maladie dont la transmission génétique est autosomique dominante, et qui… …   Wikipédia en Français

• Morbus Charcot-Marie-Tooth — Klassifikation nach ICD 10 G60.0 Hereditäre sensomotorische Neuropathie inkl. Charcot Marie Tooth Hoffmann Syndrom …   Deutsch Wikipedia