Apraxia is an isolated disorder and uncommon gestural. This
infrequent anomaly results from brain damage that can have various origins
(traumatic, infectious, etc.). Patients with apraxia have difficulty memorizing
or performing a set of movements necessary to complete simple or complex tasks,
despite having intact physical ability. The diagnosis of apraxia is
essentially clinical, but neuropsychological tests can confirm it, and its
cause specified by imaging tests. There is no cure for apraxia. Support by
physiotherapy and telehealth psychiatry services
makes it possible to adapt to the patient's environment and facilitate daily
life.
Definition and Symptoms
What is Apraxia?
The term apraxia derives from the word "praxis,"
which designates every human being's capacity to perform gestures. More or less
complex, the latter can be carried out with or without an object and be
associated or not with action. Apraxia is therefore characterized by a
difficulty in carrying out a sequence of gestures.
There are various forms of apraxia depending on the part of
the brain-injured, including ideomotor apraxia in the event of the parietal
lobe's involvement and creativity or constructive apraxia in the event
involvement of the parietal-temporal-occipital junction.
Note that agraphia (inability to write) and aphasia of
expression (impairment of speech) are also apraxia forms.
Usually, apraxia is caused by damage to the brain,
specifically the parietal lobes or nerve pathways. The affected areas of the
brain are responsible for memorizing the learned sequences of movements. These
lesions may be related to a tumor, injury, infection, vascular disease ( stroke
), or dementia.
What are The Symptoms?
Patients suffering from apraxia are no longer able to
memorize or accomplish a sequence of movements to carry out more or less
complex tasks. For example, it is difficult for them to press a button, even
though their hands are physically able to do so.
Ideomotor apraxia results in an inability to perform a
verbal command gesture when spontaneous activity and reflexes are intact. For
example, the patient cannot make the sign of the cross if asked, while he will
be able to do so spontaneously upon entering a church. Note that this type of
apraxia is associated with aphasia.
To know! Aphasia is the medical term that designates in the
individual, a partial or total loss of the capacity to express oneself or
understand the written and spoken language.
Ideational apraxia involves a disturbance in the coordination
of movement when an action requires the use of an object such as dressing or
lighting a candle, for example. The gestures are jerky and confused. It is
complicated for the patient to follow a specific course of action. This type of
apraxia is often associated with Wernicke's aphasia and homonymous lateral
hemianopsia (loss of the right or left side of the field of vision).
To know! Wernicke's aphasia is also known as receptive or
sensory aphasia. The patient can express himself, but the chosen words are
inappropriate, the sentence's construction illogical, and the flow too high,
which makes his speech incomprehensible.
Constructive apraxia is manifested by a difficulty in
apprehending the spatial relationships of objects. For example, it is difficult
for patients to graphically reproduce simple or complex figures. This apraxia
can sometimes be associated with Wernicke's aphasia.
Dynamic apraxia is characterized by an inability to perform
a sequence of rapid movements on demand according to a set schedule. For
example, the patient cannot successfully and rapidly present his fist, palm,
and finally, his hand's edge.
It also exists :
·
The apraxia of the dressing which prevents the
patient from performing actions considered to be simple or routine such as
tying their laces or buttoning their shirt;
·
Oral and facial apraxia, manifested by
difficulty in making movements with the face such as whistling or sticking out
the tongue.
Individuals with apraxia of speech are incapable of
producing the sounds fundamental to verbal expression. Indeed, patients do not
manage to initiate, coordinate, or perform the muscle movements essential to
speech.
Finally, some forms of apraxia may only affect the
performance of a few very specific tasks, such as buttoning your shirt, tying
your laces, or even picking up a phone.
Generally speaking, apraxic patients suffer from a loss of
their autonomy in daily tasks. It should be noted that the apraxia caused by a
cerebrovascular accident (CVA) evolves in a more stable way, even benefits from
an improvement of its symptoms.
Risk Factors
Abnormalities in the FOXP2 gene appear to raise the risk of
childhood apraxia of speech (CAS) and other speech and language illnesses. The
FOXP2 gene may be intricate in how certain nerves and pathways in the brain
develop. Researchers continue learning how abnormalities in the FOXP2 gene may
affect motor coordination and speech and language handling in the brain.
Complications
Various children with childhood apraxia of speech (CAS) have
other difficulties that affect their ability to communicate. These difficulties
aren't due to CAS, but they may be seen along with CAS.
Symptoms of
difficulties that are often existing along with CAS include:
Delayed languages, such as trouble understanding speech,
reduced vocabulary, or trouble using correct grammar when placing words
together in a phrase or sentence
Delays in intellectual and motor development and
difficulties with reading, spelling, and writing
Troubles with gross and fine motor movement skills or
coordination
Hypersensitivity, in which the child may not like some
textures in clothing or the texture of certain foods, or the child may not like
tooth brushing
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