Scapular winging

Abnormal protrusion of the scapula away from the surface of the back.

Also called: Scapula alata, Winged scapulae, Winged scapulas, Winged shoulder blade, Scapular weakness.

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

Conditions associated with scapular winging

The following conditions have been associated with scapular winging in medical literature. This is informational and not a diagnosis.

Adult-onset distal myopathy due to VCP mutation

Adult-onset distal myopathy due to VCP mutation is a medical condition that may be associated with various sym...

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 optic atrophy, classic form

Autosomal dominant optic atrophy, classic form is a medical condition that may be associated with various symp...

General

Autosomal recessive progressive external ophthalmoplegia

Autosomal recessive progressive external ophthalmoplegia is a medical condition that may be associated with va...

General

Bethlem muscular dystrophy

Bethlem muscular dystrophy is a medical condition that may be associated with various symptoms and signs....

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

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

Facioscapulohumeral dystrophy

Facioscapulohumeral dystrophy is a medical condition that may be associated with various symptoms and signs....

General

GNE myopathy

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

General

Immune-mediated necrotizing myopathy

Immune-mediated necrotizing myopathy is a medical condition that may be associated with various symptoms and s...

General

Morimoto-Ryu-Malicdan neuromuscular syndrome

Morimoto-Ryu-Malicdan neuromuscular syndrome is a medical condition that may be associated with various sympto...

General

Multiple acyl-CoA dehydrogenase deficiency

Multiple acyl-CoA dehydrogenase deficiency is a medical condition that may be associated with various symptoms...

General

Pure mitochondrial myopathy

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

General

Synaptic congenital myasthenic syndrome

Synaptic congenital myasthenic syndrome is a medical condition that may be associated with various symptoms an...

General

congenital myopathy 22A, classic

congenital myopathy 22A, classic is a medical condition that may be associated with various symptoms and signs...

General

congenital myopathy 23

Any nemaline myopathy in which the cause of the disease is a mutation in the TPM2 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

congenital myopathy 7A, myosin storage, autosomal dominant

congenital myopathy 7A, myosin storage, autosomal dominant is a medical condition that may be associated with ...

General

facioscapulohumeral muscular dystrophy 1

Any facioscapulohumeral muscular dystrophy associated with contraction of the D4Z4 macrosatellite repeat in th...

General

inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1

A rare autosomal dominant inherited disorder caused by mutations in the VCP gene. It can affect the muscles, b...

General

intellectual disability, autosomal dominant 52

intellectual disability, autosomal dominant 52 is a medical condition that may be associated with various symp...

General

micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome

micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome is a medical ...

General

myofibrillar myopathy 6

Selcen type muscular dystrophy is characterized by progressive limb and axial muscle weakness associated with ...

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

myopathy, myofibrillar, 9, with early respiratory failure

myopathy, myofibrillar, 9, with early respiratory failure is a medical condition that may be associated with v...

General

nemaline myopathy 5C, autosomal dominant

nemaline myopathy 5C, autosomal dominant is a medical condition that may be associated with various symptoms a...

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

sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthri...

General

trichorhinophalangeal syndrome type II

Langer-Giedon syndrome, also known as trichorhinophalangeal syndrome type 2, is a very rare, genetic, multiple...

General

Tests

Tests providers may use to investigate scapular winging

When investigating scapular winging, a healthcare provider may order one or more of the following laboratory tests. Test selection is a clinical decision made by a qualified professional.

C-Reactive Protein (CRP)

Measures inflammation in the body....

Sample: Blood

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 scapular winging

When to seek care

Seek care from a qualified healthcare provider if scapular winging 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 scapular winging mean?

Scapular winging is a health sign or symptom described in medical literature. Abnormal protrusion of the scapula away from the surface of the back.

Which conditions are associated with scapular winging?

Scapular winging has been reported in association with 33 conditions in the medical literature we index, including Adult-onset distal myopathy due to VCP mutation, Anoctamin-5-related limb-girdle muscular dystrophy R12, Autosomal dominant Charcot-Marie-Tooth disease type 2Y, Autosomal dominant optic atrophy, classic form, Autosomal recessive progressive external ophthalmoplegia. These associations do not mean you have any of these conditions.

Should I see a doctor about scapular winging?

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.

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