Hereditary spastic paraplegia 1 G11.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. 2 The 2021 edition of ICD-10-CM G11.4 became effective on October 1, 2020. 3 This is the American ICD-10-CM version of G11.4 - other international versions of ICD-10 G11.4 may differ. More ...
Diagnosis Index entries containing back-references to G11.4: Ataxia, ataxy, ataxic R27.0 ICD-10-CM Diagnosis Code R27.0 Paralysis, paralytic (complete) (incomplete) G83.9 ICD-10-CM Diagnosis Code G83.9 Paraplegia (lower) G82.20 ICD-10-CM Diagnosis Code G82.20
Diagnosis Index entries containing back-references to G82.20: Diplegia (upper limbs) G83.0 ICD-10-CM Diagnosis Code G83.0. Diplegia of upper limbs 2016 2017 2018 2019 Billable/Specific Code Paraplegia (lower) G82.20
ICD-10-CM Diagnosis Code G83.0. Diplegia of upper limbs. 2016 2017 2018 2019 2020 2021 Billable/Specific Code. Applicable To. Diplegia (upper) Paralysis of both upper limbs. lower limbs G82.20. Paraplegia (lower) G82.20. ICD-10-CM Codes Adjacent To G82.20.
HSP shares several clinical features of the progressive phase in Multiple Sclerosis (MS) which is a chronic neurodegenerative disease characterized by multiple areas of central nervous system (CNS) inflammation, demyelination and axonal loss.
The hereditary spastic paraplegias (HSP) are a large group of inherited neurologic disorders that share the primary symptom of difficulty walking due to muscle weakness and muscle tightness (spasticity) in the legs. There are more than 80 different genetic types of HSP.
Hereditary spastic paraplegia is a general term for a group of rare inherited disorders that cause weakness and stiffness in the leg muscles. Symptoms gradually get worse over time. It's also known as familial spastic paraparesis or Strümpell-Lorrain syndrome.
Hereditary spastic paraplegiaG11. 4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.The 2022 edition of ICD-10-CM G11. 4 became effective on October 1, 2021.This is the American ICD-10-CM version of G11. 4 - other international versions of ICD-10 G11.
Flaccid paralysis causes your muscles to shrink and become flabby. It results in muscle weakness. Spastic paralysis involves tight and hard muscles. It can cause your muscles to twitch uncontrollably, or spasm.
Brain MRI abnormalities, such as a thin corpus callosum, may be seen in some of the complicated forms of HSP. Several genetic mutations have been identified which underlie various forms of HSP, and specialized genetic testing and diagnosis are available at some medical centers. HSP has several forms of inheritance.
ICD-10 code G82 for Paraplegia (paraparesis) and quadriplegia (quadriparesis) is a medical classification as listed by WHO under the range - Diseases of the nervous system .
Paraparesis occurs when you're partially unable to move your legs. The condition can also refer to weakness in your hips and legs. Paraparesis is different from paraplegia, which refers to a complete inability to move your legs.
Whereas spasticity arises as a result of damage to the corticoreticulospinal (pyramidal) tracts, rigidity is caused by dysfunction of extrapyramidal pathways, most commonly the basal ganglia, but also as a result of lesions of the mesencephalon and spinal cord.
ICD-10 code G11. 4 for Hereditary spastic paraplegia is a medical classification as listed by WHO under the range - Diseases of the nervous system .
The spastic quadriparesis ICD 10 code is G82. 50 and can be used to indicate a diagnosis for reimbursement purposes.
I63. 9 - Cerebral infarction, unspecified | ICD-10-CM.
Paraplegia is also known as complete paraplegia (disorder), human T-cell lymphotropic virus (HTLV) 1-associated myelopathy-tropical spastic paraparesis (disorder), incomplete paraplegia (disorder), paraparesis, paraparesis or paraplegia as late effect of stroke (disorder), paraparesis w paraplegia, late effect of stroke, paraparesis with paraplegia due to stroke, paraplegia (complete or partial paralysis of legs), paraplegia (paralysis of legs) with neurogenic bladder, paraplegia (paralysis of legs) complete, paraplegia (paralysis of legs) incomplete, paraplegia w neurogenic bladder, paraplegia with neurogenic bladder (disorder), paraplegia complete, paraplegia incomplete, and spastic paraplegia tropical..
Paraplegia is paralysis of the lower half of the body. This is typically caused because of spinal cord injuries. Symptoms may include loss of all motor and sensory functions below the mid chest region, full dependence of a wheel chair, and having to use a stoma or catheter.
The name the laboratory assigns the test. Used as the default title of the page specific to the test.
The assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.
How likely the test is to significantly improve patient outcomes. Lab-provided.
How consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.
Paraplegia (lower) NOS. Paraplegia. Approximate Synonyms. Paralytic syndrome of both lower limbs as sequela of stroke. Paraparesis. Paraparesis with paraplegia due to stroke. Paraplegia. Paraplegia (complete or partial paralysis of legs) Paraplegia (paralysis of legs) with neurogenic bladder.
Paraplegia with neurogenic bladder. Paraplegia, late effect of stroke. Clinical Information. Complete or partial loss of movement in the lower part of the body, including both legs.
Complete paralysis of the lower half of the body including both legs, often caused by damage to the spinal cord. Paralysis of the legs and lower part of the body. Paralysis of the lower limbs and trunk. Severe or complete loss of motor function in the lower extremities and lower portions of the trunk.