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syndrome and may
They typically have similar side effects to the SSRIs, though a withdrawal syndrome on discontinuation may necessitate dosage tapering.
There is a risk of a benzodiazepine withdrawal and rebound syndrome after continuous usage for longer than two weeks, and tolerance and dependence may occur if patients stay under this treatment for longer.
Conversely, the withdrawal syndrome may also be a trigger for relapse.
Better management of the withdrawal syndrome may improve the ability of individuals to discontinue antipsychotics.
Psychosis, confusion, and organic brain syndrome may be caused by alcohol misuse, which can lead to a misdiagnosis such as schizophrenia.
Phantom sensations and phantom pain may also occur after the removal of body parts other than the limbs, e. g. after amputation of the breast, extraction of a tooth ( phantom tooth pain ) or removal of an eye ( phantom eye syndrome ).
Tolerance can develop to their effects and there is also a risk of dependence, and upon discontinuation a withdrawal syndrome may occur.
Symptoms may also occur during a gradual dosage reduction, but are typically less severe and may persist as part of a protracted withdrawal syndrome for months after cessation of benzodiazepines.
Their use by expectant mothers shortly before the delivery may result in a floppy infant syndrome, with the newborns suffering from hypotonia, hypothermia, lethargy, and breathing and feeding difficulties.
For some individuals, an obsessive compulsion to believe, prove, or re-tell a conspiracy theory may indicate one or a combination of well-understood psychological conditions, and other hypothetical ones: paranoia, denial, schizophrenia, mean world syndrome.
With sinus node dysfunction ( sometimes called sick sinus syndrome ), there may be disordered automaticity or impaired conduction of the impulse from the sinus node into the surrounding atrial tissue ( an " exit block ").
Carbamazepine may cause syndrome of inappropriate antidiuretic hormone ( SIADH ), since it both increases the release and potentiates the action of ADH ( vasopressin ).
Chlamydia may also cause reactive arthritis ( reiter's syndrome )-the triad of arthritis, conjunctivitis and urethritis ( inflammation of the urethra )-especially in young men.
The patient may experience locked-in syndrome where cognitive function is intact, but all muscles are paralyzed with the exception of eye blinking.
NBTE may also occur in patients with cancers, particularly mucinous adenocarcinoma where Trousseau syndrome can be encountered.
She described this condition in 1978 Estimates of the prevalence of this rare disorder have ranged from 1: 20, 000 to 1: 40, 000 births, though the incidence may be found to be greater as the syndrome becomes better recognized and new genetic evidence is discovered.
: Additional features that are seen in significant numbers of patients with Dravet syndrome may include sensory integration disorders and other autism spectrum characteristics, orthopedic or movement disorders, frequent or chronic upper respiratory and ear infections, sleep disturbance, dysautonomia, and problems with growth and nutrition.
West syndrome may arise from idiopathic, symptomatic, or cryptogenic causes.
In general, most surviving patients remain with significant cognitive impairment and continuing seizures and may evolve to another eponymic syndrome, Lennox-Gastaut syndrome.
Recurrent mild hypoglycemia may fit a reactive hypoglycemia pattern, but this is also the peak age for idiopathic postprandial syndrome, and recurrent " spells " in this age group can be traced to orthostatic hypotension or hyperventilation as often as demonstrable hypoglycemia.
It is reported that high ammonia and / or high nitrogen levels may occur with high protein intake, excessive aluminum exposure, Reye's syndrome, cirrhosis, and urea cycle disorder.
A chest CT-scan showing a thymoma ( red circle ) A chest X-ray is frequently performed ; it may point towards alternative diagnoses ( e. g. Lambert-Eaton syndrome due to a lung tumor ) and comorbidity.

syndrome and be
Optic ataxia is usually part of Balint's syndrome, but can be seen in isolation with injuries to the superior parietal lobule, as it represents a disconnection between visual-association cortex and the frontal premotor and motor cortex, and ataxic respiration ( lack of coordination in respiratory movements, usually due to dysfunction of the respiratory centres in the medulla oblongata ).
Excess calcium from supplements, fortified food and high-calcium diets, can cause milk-alkali syndrome, which has serious toxicity and can be fatal.
AVM is not generally thought to be an inherited disorder, unless in the context of a specific hereditary syndrome.
To test the developing fetus for Down syndrome, Amniocentesis and chorionic villus sampling can be used.
Restless legs syndrome can be treated using clonazepam as a third line treatment option as the use of clonazepam is still investigational.
Antipsychotics should be used with care as they can worsen catatonia and are the cause of neuroleptic malignant syndrome, a dangerous condition that can mimic catatonia and requires immediate discontinuation of the antipsychotic.
Alpers ' syndrome in infants is also thought to be a transmissible spongiform encephalopathy caused by a prion.
The FDA informed health care professionals that dangerous or even fatal skin reactions ( Stevens – Johnson syndrome and toxic epidermal necrolysis ), that can be caused by carbamazepine therapy, are significantly more common in patients with a particular human leukocyte antigen ( HLA ) allele, HLA-B * 1502.
They are often portrayed as children with Williams syndrome ( which was not recognised as a medical condition but some specialist believe that people were enchanted with their character and appearance that they believed to be magical ), usually with fair hair.
There are four main groups of epileptic syndrome which can be further divided into: benign Rolandic epilepsy, frontal lobe epilepsy, infantile spasms, juvenile myoclonic epilepsy, juvenile absence epilepsy, childhood absence epilepsy ( pyknolepsy ), hot water epilepsy, Lennox-Gastaut syndrome, Landau-Kleffner syndrome, Dravet syndrome, progressive myoclonus epilepsies, reflex epilepsy, Rasmussen's syndrome, temporal lobe epilepsy, limbic epilepsy, status epilepticus, abdominal epilepsy, massive bilateral myoclonus, catamenial epilepsy, Jacksonian seizure disorder, Lafora disease, photosensitive epilepsy, etc.
What can be even more confusing is that certain syndromes, such as West syndrome, featuring seizures such as infantile spasms, can be classified as idiopathic, syndromic, or cryptogenic depending on cause and can arise from both focal or generalized epileptic lesions.
Idiopathic postprandial syndrome without demonstrably low glucose levels at the time of symptoms can be more of a management challenge.

syndrome and hard
There are many diseases similar to Binswanger disease including CADASIL syndrome and Alzheimer's disease which makes this specific type of white matter damage hard to diagnose.
Diagnosis of post-polio syndrome can be difficult, since the symptoms are hard to separate from complications due to the original poliomyelitis infection, and from the normal infirmities of aging.
Dyspraxics may have characteristics of dyslexia ( difficulty with reading and spelling ), dyscalculia ( difficulty with mathematics ), dysgraphia ( an inability to write neatly and / or draw ) expressive language disorder ( difficulty with verbal expression ), ADHD ( poor attention span and impulsive behaviour ), or Asperger syndrome ( consisting variously of poor social cognition, a literal understanding of language it hard to understand idioms or sarcasm, and rigid, intense interests ).
Abbruzzese is also known to be a particularly hard hitter, which may be reflected in him having suffered from carpal tunnel syndrome at one time.
Amniotic band syndrome is often difficult to detect before birth as the individual strands are small and hard to see on ultrasound.
The common symptoms in all reported cases of primrose syndrome include ossified pinnae, learning disabilities or mental retardation, hearing problems, movement disorders ( ataxia, paralysis, and parkinsonism among others ( likely due, in part, to calcification of the basal ganglia ), a torus palatinus ( a neoplasm on the mouth's hard palate ), muscle atrophy, and distorted facial features.
The difference that the 70s ' " Teeny Bopper syndrome " had with prior idol phenomena was that these new teen idols were directed at even younger girls, down to 15 years old, who were too young to have heard The Beatles and were not attracted to the new hard rock music of the time that their elder siblings listened to.

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