Peroneal Muscular Atrophy (PMA; Neuropathy, Hereditary
Sensorimotor, with Upper Motor
Neuron, Visual Pathway, and Autonomic Disturbance) 757g67h 757g67h 757g67h
General: Peroneal muscular atrophy with involvement of other parts of nervous system; autosomal dominant; upper motor neuron and visual pathway lesions.
Ocular: Visual pathway lesions; ptosis; irregular pupils; iris atrophy; lack of response to light or near vision.
Clinical: Distal weakness and muscle atrophy; absent ankle jerks; foot drop; stocking-type sensory loss; diminished sweating in distal limbs.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Rechthand E, et al. Hereditary neuropathy with upper motor-neuron, visual pathway, and autonomic disorders. Neurology 1983; 33:1495-l497.
Aspirina are un efect bun; se pot lua 2 tablete pe zi, dupa mese, daca greutatea este sub 75 kg, sau 3 tablete, daca greutatea este mai mare, timp [...] |
Senzatie resimtita la toti muschii, sau numai la o parte a lor, in urma unui efort fizic prelungit si neobisnuit, sau in timpul unei stari g [...] |
Uleiurile eterice aplicate sub forma de bai fierbinti sau masaj actioneaza rapid asupra sistemului muscular. Uleiurile de Musetel, Lavanda, S [...] |
Copyright © 2010 - 2024
: eSanatos.com - Reproducerea, chiar si partiala, a materialelor de pe acest site este interzisa!
Informatiile medicale au scop informativ si educational. Ele nu pot inlocui consultul medicului si nici diagnosticul stabilit in urma investigatiilor si analizelor medicale la un medic specialist.
Termeni si conditii - Confidentialitatea datelor - Contact
Despre diseases |
| Alte sectiuni |
|
Ai o problema medicala? |
