Proximal upper limb muscle weakness

A lack of strength of the proximal muscles of the arms.

Also called: Proximal muscle weakness in upper limbs.

Not sure what proximal upper limb muscle weakness might be related to? See the lab tests that healthcare providers may use to investigate proximal upper limb muscle weakness, and the conditions they help explore.
Explore relevant lab tests
Associations

Conditions associated with proximal upper limb muscle weakness

The following conditions have been associated with proximal upper limb muscle weakness in medical literature. This is informational and not a diagnosis.

Acute intermittent porphyria

Acute intermittent porphyria is a medical condition that may be associated with various symptoms and signs....

General

Anoctamin-5-related limb-girdle muscular dystrophy R12

Anoctamin-5-related limb-girdle muscular dystrophy R12 is a medical condition that may be associated with vari...

General

Autosomal dominant Charcot-Marie-Tooth disease type 2Y

Autosomal dominant Charcot-Marie-Tooth disease type 2Y is a medical condition that may be associated with vari...

General

Autosomal dominant Charcot-Marie-Tooth disease type 2Z

Autosomal dominant Charcot-Marie-Tooth disease type 2Z is a medical condition that may be associated with vari...

General

Autosomal dominant centronuclear myopathy

Autosomal dominant centronuclear myopathy is a medical condition that may be associated with various symptoms ...

General

Autosomal recessive Charcot-Marie-Tooth disease with hoarseness

Autosomal recessive Charcot-Marie-Tooth disease with hoarseness is a medical condition that may be associated ...

General

Centronuclear myopathy 1

Centronuclear myopathy 1 is a medical condition that may be associated with various symptoms and signs....

General

Charcot-Marie-Tooth disease axonal type 2C

Autosomal dominant Charcot-Marie-Tooth disease type 2C (CMT2C) is a form of axonal Charcot-Marie-Tooth disease...

General

Charcot-Marie-Tooth disease type 1F

Charcot-Marie-Tooth disease type 1F is a medical condition that may be associated with various symptoms and si...

General

Charcot-Marie-Tooth disease type 4B2

Charcot-Marie-Tooth disease type 4B2 is a medical condition that may be associated with various symptoms and s...

General

Charcot-Marie-tooth disease, axonal, type 2JJ

Charcot-Marie-tooth disease, axonal, type 2JJ is a medical condition that may be associated with various sympt...

General

Dysferlin-related limb-girdle muscular dystrophy R2

Dysferlin-related limb-girdle muscular dystrophy R2 is a medical condition that may be associated with various...

General

Emery-Dreifuss muscular dystrophy 2, autosomal dominant

Emery-Dreifuss muscular dystrophy inherited in an autosomal dominant pattern and caused by mutations in the LM...

General

GMPPB-related limb-girdle muscular dystrophy R19

GMPPB-related limb-girdle muscular dystrophy R19 is a medical condition that may be associated with various sy...

General

Genetic recurrent myoglobinuria

Genetic recurrent myoglobinuria is a medical condition that may be associated with various symptoms and signs....

General

Hereditary coproporphyria

Hereditary coproporphyria is a medical condition that may be associated with various symptoms and signs....

General

Late-onset distal myopathy, Markesbery-Griggs type

Late-onset distal myopathy, Markesbery-Griggs type is a medical condition that may be associated with various ...

General

Oculopharyngodistal myopathy

Oculopharyngodistal myopathy is a medical condition that may be associated with various symptoms and signs....

General

Variegate porphyria

Variegate porphyria is a medical condition that may be associated with various symptoms and signs....

General

congenital myasthenic syndrome 9

Any congenital myasthenic syndrome in which the cause of the disease is a mutation in the MUSK gene....

General

congenital myopathy 25

congenital myopathy 25 is a medical condition that may be associated with various symptoms and signs....

General

congenital myopathy 26

congenital myopathy 26 is a medical condition that may be associated with various symptoms and signs....

General

frontotemporal dementia and/or amyotrophic lateral sclerosis 6

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the VCP gene....

General

muscular dystrophy, limb-girdle, autosomal recessive 28

muscular dystrophy, limb-girdle, autosomal recessive 28 is a medical condition that may be associated with var...

General

muscular dystrophy, limb-girdle, autosomal recessive 29

muscular dystrophy, limb-girdle, autosomal recessive 29 is a medical condition that may be associated with var...

General

myopathy, distal, 7, adult-onset, X-linked

myopathy, distal, 7, adult-onset, X-linked is a medical condition that may be associated with various symptoms...

General

myopathy, myofibrillar, 13, with rimmed vacuoles

A rare genetic neuromuscular disease caused by a mutation in HSPB8 gene, characterized by length-dependent axo...

General

neuronopathy, distal hereditary motor, autosomal recessive 7

neuronopathy, distal hereditary motor, autosomal recessive 7 is a medical condition that may be associated wit...

General

oculopharyngodistal myopathy 5

oculopharyngodistal myopathy 5 is a medical condition that may be associated with various symptoms and signs....

General

Tests

Tests providers may use to investigate proximal upper limb muscle weakness

When investigating proximal upper limb muscle weakness, a healthcare provider may order one or more of the following laboratory tests. Test selection is a clinical decision made by a qualified professional.

CBC with Differential

Measures red blood cells, white blood cells, and platelets to help evaluate overall health and detect disorder...

Sample: Blood

Comprehensive Metabolic Panel (CMP)

Measures 14 substances in the blood to assess kidney and liver function, electrolyte balance, and blood sugar ...

Sample: Blood

Urinalysis

Examines urine content to help detect urinary tract infections, kidney disease, and diabetes....

Sample: Urine

Related

Symptoms commonly seen alongside proximal upper limb muscle weakness

When to seek care

Seek care from a qualified healthcare provider if proximal upper limb muscle weakness is severe, persistent, worsening, or accompanied by concerning symptoms. If you think you have a medical emergency, call your local emergency number immediately.

FAQ

Frequently Asked Questions

What does the symptom proximal upper limb muscle weakness mean?

Proximal upper limb muscle weakness is a health sign or symptom described in medical literature. A lack of strength of the proximal muscles of the arms.

Which conditions are associated with proximal upper limb muscle weakness?

Proximal upper limb muscle weakness has been reported in association with 29 conditions in the medical literature we index, including Acute intermittent porphyria, Anoctamin-5-related limb-girdle muscular dystrophy R12, Autosomal dominant Charcot-Marie-Tooth disease type 2Y, Autosomal dominant Charcot-Marie-Tooth disease type 2Z, Autosomal dominant centronuclear myopathy. These associations do not mean you have any of these conditions.

Should I see a doctor about proximal upper limb muscle weakness?

You should discuss any persistent or concerning symptoms with a qualified healthcare provider. This website does not provide diagnosis. If you have severe symptoms or signs of a medical emergency, seek care immediately.

Educational content only: The information on Symptom Database.com is for educational purposes and is not medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider. Read our full disclaimer.