SAEVA Proceedings 2018 4. Proceedings | Page 138

SAEVA Congress 2018 Proceedings | 12-15 February 2018 | ATKV Goudini Spa 2. Poor physical status; i.e., weight loss 3. Laryngeal paresis and vagal signs if CN X. 4. slap test - afferent: segmental dorsal thoracic nerves, cervical spinal cord white matter to the vagal nucleus in the medulla oblongata (contralateral) - efferent: vagus nerve to recurrent laryngeal n. I. Hypoglossal (XII - motor to tongue): Grasp tongue and pull gently to check for weakness and atrophy. J. Accessory (XI) – input in swallowing and motor to trapezius and cranial sternocephalicus III. Gait and Posture If evidence of a lesion has been detected in the examination of the head (head signs), then an attempt is made to explain any abnormalities found in the rest of the examination by such a lesion above the level of the atlanto-occipital junction. If this cannot be done, then there must be at least 2 lesions, or a diffuse disease. If “head signs” are not found, the lesion(s) is assumed to be in the spinal cord, peripheral nerves, or muscles. The motor system can be evaluated more objectively than can the sensory system. Many lesions of the nervous system affect the motor system. Lesions might be single-focal, single-diffuse, or multifocal. Motor deficit, when present, is of extreme value in the localization of the lesion(s). In evaluating the motor system, it is important to understand what is meant by upper motor neuron disease and lower motor neuron disease, and be able to recognize the signs associated with each. The lower motor neuron (LMN) is a neuron whose cell body is in the ventral gray column or in specific cranial nerve nuclei and whose axon projects into the peripheral nervous system. It is the final motor unit to the effector organ. It is responsible for maintaining tone, for reflexes, and voluntary and involuntary motor function. Lower motor neuron disease would result from lesions involving spinal cord ventral gray matter, motor cranial nerve nuclei and trunks, ventral (motor) spinal roots, peripheral nerve trunks, and myoneural junctions. Signs of LMN disease include: 1. Motor deficit – partial or complete 133