"Apraxias" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7)
Descriptor ID |
D001072
|
MeSH Number(s) |
C10.597.606.881.350 C23.888.592.604.882.350 F01.700.875.350
|
Concept/Terms |
Apraxias- Apraxias
- Dyspraxia
- Dyspraxias
- Apraxia
Apraxia, Articulatory- Apraxia, Articulatory
- Apraxias, Articulatory
- Articulatory Apraxia
- Articulatory Apraxias
- Dyspraxia, Articulatory
- Articulatory Dyspraxia
- Articulatory Dyspraxias
- Dyspraxias, Articulatory
Apraxia, Developmental Verbal- Apraxia, Developmental Verbal
- Apraxias, Developmental Verbal
- Developmental Verbal Apraxia
- Developmental Verbal Apraxias
- Verbal Apraxia, Developmental
- Verbal Apraxias, Developmental
- Speech-Language Disorder 1
- 1s, Speech-Language Disorder
- Disorder 1, Speech-Language
- Disorder 1s, Speech-Language
- Speech Language Disorder 1
- Speech-Language Disorder 1s
- Developmental Verbal Dyspraxia
- Developmental Verbal Dyspraxias
- Dyspraxia, Developmental Verbal
- Dyspraxias, Developmental Verbal
- Verbal Dyspraxia, Developmental
- Verbal Dyspraxias, Developmental
Apraxia, Facial-Oral- Apraxia, Facial-Oral
- Apraxia, Facial Oral
- Apraxias, Facial-Oral
- Facial-Oral Apraxia
- Facial-Oral Apraxias
- Speech And Language Disorder With Orofacial Dyspraxia
Ideational Apraxia- Ideational Apraxia
- Apraxia, Ideational
- Apraxias, Ideational
- Ideational Apraxias
Apraxia, Motor- Apraxia, Motor
- Apraxias, Motor
- Motor Apraxia
- Motor Apraxias
Apraxia, Oral- Apraxia, Oral
- Apraxias, Oral
- Oral Apraxia
- Oral Apraxias
- Dyspraxia, Oral
- Dyspraxias, Oral
- Oral Dyspraxia
- Oral Dyspraxias
Apraxia, Verbal- Apraxia, Verbal
- Apraxias, Verbal
- Verbal Apraxia
- Verbal Apraxias
- Dyspraxia, Verbal
- Dyspraxias, Verbal
- Verbal Dyspraxia
- Verbal Dyspraxias
Dressing Apraxia- Dressing Apraxia
- Apraxia, Dressing
- Apraxias, Dressing
- Dressing Apraxias
Apraxia, Gestural- Apraxia, Gestural
- Apraxias, Gestural
- Gestural Apraxia
- Gestural Apraxias
|
Below are MeSH descriptors whose meaning is more general than "Apraxias".
Below are MeSH descriptors whose meaning is more specific than "Apraxias".
This graph shows the total number of publications written about "Apraxias" by people in this website by year, and whether "Apraxias" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2020 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Apraxias" by people in Profiles.
-
Behavioral Treatment for Speech and Language in Primary Progressive Aphasia and Primary Progressive Apraxia of Speech: A Systematic Review. Neuropsychol Rev. 2024 Sep; 34(3):882-923.
-
A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech. Nat Commun. 2021 06 08; 12(1):3452.
-
Speech and Language Presentations of FTLD-TDP Type B Neuropathology. J Neuropathol Exp Neurol. 2020 03 01; 79(3):277-283.
-
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome. Eur J Hum Genet. 2013 Apr; 21(4):455-9.
-
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization. Genet Med. 2012 Nov; 14(11):928-36.
-
Phenotype of FOXP2 haploinsufficiency in a mother and son. Am J Med Genet A. 2012 Jan; 158A(1):174-81.
-
Isolated eyelid-opening apraxia: report of a new levodopa-responsive syndrome. Neurology. 1994 Sep; 44(9):1752-4.