Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Polyneuropathy

View through CrossRef
Typically polyneuropathy will cause the combination of distal limb muscle weakness, loss of tendon reflexes, and reduced distal limb sensation. There is variable involvement of the autonomic innervation, damage to which causes a dry, vasodilated foot or hand. Loss of tendon reflexes is a cardinal sign of polyneuropathy, often restricted to the ankle jerks in axonal degeneration, but involving more proximal reflexes in acquired demyelinating neuropathies which may involve more proximal segments or the nerve roots. Clinical features suggestive of demyelinating or conduction block polyneuropathy include: a relative lack of muscle wasting in relation to the degree of weakness because no denervation has occurred; weakness of proximal muscles as well as distal, because of nerve root involvement; and disproportionate loss of joint position and vibration sensations compared to relative preservation of pain and temperature sensations which are carried by unmyelinated fibres.
Title: Polyneuropathy
Description:
Typically polyneuropathy will cause the combination of distal limb muscle weakness, loss of tendon reflexes, and reduced distal limb sensation.
There is variable involvement of the autonomic innervation, damage to which causes a dry, vasodilated foot or hand.
Loss of tendon reflexes is a cardinal sign of polyneuropathy, often restricted to the ankle jerks in axonal degeneration, but involving more proximal reflexes in acquired demyelinating neuropathies which may involve more proximal segments or the nerve roots.
Clinical features suggestive of demyelinating or conduction block polyneuropathy include: a relative lack of muscle wasting in relation to the degree of weakness because no denervation has occurred; weakness of proximal muscles as well as distal, because of nerve root involvement; and disproportionate loss of joint position and vibration sensations compared to relative preservation of pain and temperature sensations which are carried by unmyelinated fibres.

Related Results

Acute Inflammatory Demyelinating Polyneuropathy (Guillain-Barré Syndrome)
Acute Inflammatory Demyelinating Polyneuropathy (Guillain-Barré Syndrome)
Acute inflammatory demyelinating polyneuropathy (AIDP), also known as Guillain-Barré syndrome (GBS), is a common acute neurological presentation encountered in both the outpatient ...
Demyelinating Diseases 2: NMO, ADEM, GBS, CIDP (DRAFT)
Demyelinating Diseases 2: NMO, ADEM, GBS, CIDP (DRAFT)
The video in this chapter explores demyelinating diseases, and focuses on neuromyelitis optica (NMO), acute disseminated encephalomyelitis (ADEM), Guillain-Barré syndrome (GBS) and...
Proximal Arm Weakness
Proximal Arm Weakness
Proximal arm muscles include supra and infra spinatii, pectoralis major and minor, teres major and minor, rhomboids, serratus anterior, deltoids, biceps, and triceps. The main func...
Peripheral Nervous System 1: Neuropathy (DRAFT)
Peripheral Nervous System 1: Neuropathy (DRAFT)
The video in this chapter explores the peripheral nervous system (PNS) and focuses on neuropathy. It outlines classifications of PNS injury (by process, etiology, distribution, aff...
Proximal Leg Weakness
Proximal Leg Weakness
Proximal leg weakness is a common presentation to neuromuscular clinics. Hip flexion, abduction, adduction, and rotation is mainly achieved by the iliopsoas, glutei, and obturator ...
Peripheral Nerve Biopsy
Peripheral Nerve Biopsy
Nerve biopsy is an important part of the diagnostic armamentarium in the evaluation of a number of diseases, including vasculitis, some hereditary neuropathies, toxic and metabolic...
Dyspnea
Dyspnea
The most common causes of dyspnea are not neuromuscular but rather are cardiac and pulmonary. However, dyspnea is an important and serious manifestation of many neuromuscular disor...
Gangliosidoses (GM1 and GM2)
Gangliosidoses (GM1 and GM2)
GM1 gangliosidosis is due to beta-galactosidase deficiency. The adult-onset form is characterized by progressive generalized dystonia, often associated with akineto-rigid Parkinson...

Back to Top