Muscle Weakness and Atrophy: Causes & Reasons

Possible Causes for Muscle Weakness and Atrophy

weakness Muscle Atrophy Movement difficulty Spasticity Excess saliva from reduced swallowing Thicker saliva may sometimes be difficult to clear from the chest or throat due [physio-pedia.com]

The altered axons may impair transmission of impulses from nerves to muscles, leading to muscle weakness and atrophy. [ghr.nlm.nih.gov]

It is characterized by weakness, spasticity and muscle atrophy and is fatal in most cases. [medical-dictionary.thefreedictionary.com]

Progressive Muscular Atrophy

She developed muscle weakness of the distal part of the left lower extremity at age 42, followed by muscle weakness and atrophy of the right lower extremity and upper extremities [ncbi.nlm.nih.gov]

Signs and symptoms include muscle weakness, atrophy, and fasciculation Group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting [icd9data.com]

Without adequate nerve function, patients with SMA experience progressive muscle weakness and atrophy, impacting the ability to crawl, sit, or stand and eventually to breathe [rdmag.com]

Spinal and Bulbar Muscular Atrophy

Physical therapy and rehabilitation to slow muscle weakness and atrophy may prove helpful. [ninds.nih.gov]

Abstract Spinal and bulbar muscular atrophy (SBMA) is an adult-onset neurodegenerative disease characterized by slowly progressive muscle weakness and atrophy. [ncbi.nlm.nih.gov]

Abstract Spinal and bulbar muscular atrophy (SBMA) is the first member identified among polyglutamine diseases characterized by slowly progressive muscle weakness and atrophy [ncbi.nlm.nih.gov]

X-linked Distal Spinal Muscular Atrophy Type 3

Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord. [patient.info]

Most commonly affects the bulbar muscles with fluctuating generalized weakness. [12] Spinal Muscular Atrophy- Presents with weakness and atrophy in the limbs, respiratory, [physio-pedia.com]

Without these important parts of the brain and spinal cord, an affected person loses control of muscle movement, has muscle weakness, and loses muscle tissue (atrophy). [diseaseinfosearch.org]

Distal Spinal Muscular Atrophy Type 5

Definition A neurodegenerative disorder characterized by young adult onset of proximal muscle weakness and atrophy, muscle cramps, and fasciculations, with later onset of [uniprot.org]

Get Update Overview HMSNO is an autosomal dominant neurodegenerative disorder characterized by young adult onset of proximal or distal muscle weakness and atrophy, muscle [diseaseinfosearch.org]

OBJECTIVE: Distal hereditary motor neuropathies (dHMN) form a clinically and genetically heterogeneous group of disorders, characterized by muscle weakness and atrophy predominating [ncbi.nlm.nih.gov]

Upper Motor Neuron Disease

Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy. [advancedpsy.com]

Symptoms vary in severity and may include muscle weakness and atrophy, fasciculations, emotional lability, and respiratory muscle weakness. [msdmanuals.com]

[…] causes muscle weakness, muscle atrophy (shrinkage of muscles) and twitching (fasciculations). [mda.org]

Distal Spinal Muscular Atrophy Type 4

Symptoms vary in severity and may include muscle weakness and atrophy, fasciculations, emotional lability, and respiratory muscle weakness. [msdmanuals.com]

Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord. [patient.info]

muscle weakness. [neuropathology-web.org]

Distal Spinal Muscular Atrophy Type 1

weakness and atrophy (in lower limbs especially). [orpha.net]

In addition to muscle weakness and atrophy, a major complication of SMARD1 is breathing problems. [diseaseinfosearch.org]

[…] characterized by severe respiratory distress/respiratory failure in association with diaphragmatic eventration and palsy, as well as progressive, symmetrical, distal-to-proximal muscle [orpha.net]

Distal Spinal Muscular Atrophy Type 3

It is a gradually progressive neuromuscular disorder in adult men.Proximal muscle weakness, muscle atrophy, and fasciculations may resulted due to degeneration of lower motor [explainmedicine.com]

Without these important parts of the brain and spinal cord, an affected child loses control of muscle movement, has muscle weakness, and loses muscle tissue (atrophy). [diseaseinfosearch.org]

Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord. [patient.info]

Distal Hereditary Motor Neuropathy Type 1

weakness and atrophy. [cambridge.org]

Charcot-Marie-Tooth hereditary neuropathy type 2 (CMT2) is a non-demyelinating (axonal) peripheral neuropathy characterized by distal muscle weakness and atrophy, mild sensory [bcbst.com]

Distal hereditary motor neuropathy, type V (DHMN5) is unusual in that muscle weakness and wasting (atrophy) is experienced primarily in the hands. [thinkgenetic.com]

Limb-Girdle Muscular Dystrophy Type 2G

weakness and atrophy. [malacards.org]

A rare autosomal recessive degenerative myopathy (OMIM:601954) characterised by proximal and distal muscle weakness and atrophy in the limbs, dystrophic changes on muscle [medical-dictionary.thefreedictionary.com]

UniProtKB/Swiss-Prot : 75 Limb-girdle muscular dystrophy 2G: An autosomal recessive degenerative myopathy characterized by proximal and distal muscle weakness and atrophy [malacards.org]

Limb-Girdle Muscular Dystrophy Type 1G

weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. [orpha.net]

Muscle weakness and atrophy are usually confined to the anterior compartment of the lower leg, in particular the tibialis anterior muscle. [binfo.ncku.edu.tw]

[…] dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle [orpha.net]

Emery-Dreifuss Muscular Dystrophy Type 2

weakness and atrophy (initially with a humero-peroneal distribution but later becoming more diffuse); joint contractures of the Achilles, elbow, and neck tendons, beginning [link.springer.com]

RESULTS: The proband had typical clinical manifestation of EDMD: joint contracture, progressive muscle weakness and atrophy and cardiac conduction dysfunction. [pesquisa.bvsalud.org]

It presents slowly progressive muscle weakness and atrophy (initially and generally with a humeroperoneal distribution but later becoming more diffuse). [orpha.net]

Muscular Dystrophy-Dystroglycanopathy Type C3

weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. [orpha.net]

Limb-girdle muscular dystrophy (LGMD) is an inherited group of disorders that cause arm and leg muscle weakness and atrophy. [muscle.ca]

Miyoshi myopathy is characterized by muscle weakness and atrophy in young adults, most marked in the distal parts of the legs. [egl-eurofins.com]

Jankovic Rivera Syndrome

The muscles in the upper limbs are later affected, and soon the muscle weakness and atrophy spreads throughout the body. [ghr.nlm.nih.gov]

Genetics Home Reference Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is a neurological condition that causes muscle weakness and wasting (atrophy) [rarediseases.oscar.ncsu.edu]

Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is a neurological condition that causes muscle weakness and wasting (atrophy) and a combination of seizures [ghr.nlm.nih.gov]

Emery-Dreifuss Muscular Dystrophy Type 1

weakness and atrophy (initially with a humero-peroneal distribution but later becoming more diffuse); joint contractures of the Achilles, elbow, and neck tendons, beginning [link.springer.com]

Chapter First Online: 27 June 2014 Abstract Emery-Dreifuss muscular dystrophy (EDMD) is a progressive myopathy characterized by a clinical triad including slowly progressive muscle [link.springer.com]

First Online: 06 October 2017 Abstract Emery-Dreifuss muscular dystrophy (EDMD) is a progressive myopathy characterized by a clinical triad including slowly progressive muscle [link.springer.com]

Limb-Girdle Muscular Dystrophy Type 2C

weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. [orpha.net]

Overview Limb-girdle muscular dystrophy type 2C: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of [checkorphan.org]

[…] dystrophy type 2C (LGMD2C) is a subtype of autosomal recessive limb-girdle muscular dystrophy characterized by a childhood onset of progressive shoulder and pelvic girdle muscle [orpha.net]

Distal Myopathy Type 3

Over a period of years, the weakness and atrophy typically spread to the thighs and gluteal muscles. [rarediseases.info.nih.gov]

Other cases are disabling and severe Pelvic muscle weakness and atrophy associated with pseudohypertrophy of the calves. [icd9data.com]

As Miyoshi myopathy slowly worsens, the muscle weakness and atrophy spread up the leg to the muscles in the thigh and buttock and can also involve the upper arm and shoulder [ghr.nlm.nih.gov]

Autosomal Recessive Limb-Girdle Muscular Dystrophy

weakness and atrophy frequently associated with calf hypertrophy, diaphragmatic weakness, and/or variable cardiac abnormalities. [orpha.net]

Limb-girdle muscular dystrophy (LGMD) is an inherited group of disorders that cause arm and leg muscle weakness and atrophy. [muscle.ca]

Overview Limb-girdle muscular dystrophy type 2C: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of [checkorphan.org]

Limb-Girdle Muscular Dystrophy Type 1E

Overview Limb-girdle muscular dystrophy type 2C: An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of [checkorphan.org]

Becker muscular dystrophy is clinically characterized by the following: Progressive symmetric muscle weakness and atrophy with calf hypertrophy In some cases quadriceps femoris [centogene.com]

Affected individuals have developed severe intellectual disability, hypotonia, developmental delays, mild contractures, and muscle weakness and degeneration (atrophy). [rarediseases.org]

Distal Spinal Muscular Atrophy

Physical examination revealed atrophy and weakness of small hand muscles and mild atrophy and weakness of the lower limbs. [ncbi.nlm.nih.gov]

We present the case of a female patient, of 37-years-old, with distal muscle weakness and atrophy beginning in childhood and slowly progressive in the first two decades of [ncbi.nlm.nih.gov]

Abstract Distal hereditary motor neuropathies (distal HMNs) are characterised by degeneration of anterior horn cells of the spinal cord resulting in muscle weakness and atrophy [ncbi.nlm.nih.gov]

Charcot-Marie-Tooth Disease Type 2S

weakness and atrophy. [medical-dictionary.thefreedictionary.com]

Definition An axonal form of Charcot-Marie-Tooth disease, a disorder of the peripheral nervous system, characterized by progressive weakness and atrophy, initially of the [uniprot.org]

Symptoms typically include progressive distal muscle weakness and atrophy, often associated with mild to moderate sensory loss, depressed tendon reflexes, and high-arched [flybase.org]

Brachial Plexus Neuritis

After a few weeks the constant pain goes away and is replaced by muscle weakness or atrophy in the upper arm. [goldlawfirm.net]

Within a few hours or days of the condition’s onset, affected individuals may experience muscle weakness, wasting (atrophy), numbness (hyperesthesia), and paralysis of the [diseasesatoz.com]

weakness Muscle-atrophy (within a month) Scapular winging may be seen when there is involvement of the scapulothoracic nerve innervating the serratus anterior muscle. [physio-pedia.com]

Progressive Bulbar Paralysis

Symptoms vary in severity and may include muscle weakness and atrophy, fasciculations, emotional lability, and respiratory muscle weakness. [msdmanuals.com]

When anterior horn cells of spinal (not cranial) nerves are affected, as in spinal muscular atrophies, symptoms usually include muscle weakness and atrophy, fasciculations [merckmanuals.com]

Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy. [advancedpsy.com]

Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is a genetic neuromuscular disease characterized by progressive muscle weakness and atrophy. [ncbi.nlm.nih.gov]

weakness and atrophy. [medicinenet.com]

Abstract Paediatric motor neuron diseases encompass a group of neurodegenerative diseases characterised by the onset of muscle weakness and atrophy before the age of 18 years [ncbi.nlm.nih.gov]

Adult Spinal Muscular Atrophy

muscle weakness and atrophy. [uniprot.org]

[…] proximal muscle weakness and atrophy. [medical-dictionary.thefreedictionary.com]

About Spinal Muscular Atrophy (SMA) About SMA Spinal Muscular Atrophy (SMA) refers to a group of genetic conditions that cause muscle weakness and atrophy in children and [griswoldhomecare.com]

Limb-Girdle Muscular Dystrophy Type 2Q

Autosomal recessive limb-girdle muscular dystrophy-17 is characterized by early childhood onset of proximal muscle weakness and atrophy without skin involvement. [ncbi.nlm.nih.gov]

Miyoshi myopathy is characterized by muscle weakness and atrophy in young adults, most marked in the distal parts of the legs. [egl-eurofins.com]

Becker muscular dystrophy is clinically characterized by the following: Progressive symmetric muscle weakness and atrophy with calf hypertrophy In some cases quadriceps femoris [centogene.com]

Limb-Girdle Muscular Dystrophy Type 2E

Overview An autosomal recessive form of limb-girdle muscular dystrophy where muscle weakness and atrophy is caused by mutations of the beta-sarcoglycan gene. [checkorphan.org]

It is characterized by early weakness and atrophy of the pelvic and shoulder girdle muscles in adolescence or young adulthood, with slow progression. [jewishgeneticdiseases.org]

It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. [fpnotebook.com]

Spinal Muscular Atrophy Type 4

SMA's an autosomal recessive disorder that causes alpha motor neurons in the spinal cord to die, resulting in muscle weakness and atrophy. [youtube.com]

Citation metadata Abstract : Spinal muscular atrophy (SMA) is a neuromuscular disorder Characterized by progressive proximal manifestation of muscle Weakness and atrophy. [go.gale.com]

[…] anterior horn cells of the spinal cord, leading to symmetrical muscle weakness and atrophy. [malacards.org]

Lower Motor Neuron Syndrome with Late-Adult Onset

Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy. [advancedpsy.com]

Symptoms vary in severity and may include muscle weakness and atrophy, fasciculations, emotional lability, and respiratory muscle weakness. [msdmanuals.com]

[…] causes muscle weakness, muscle atrophy (shrinkage of muscles) and twitching (fasciculations). [mda.org]