** Wolff-Parkinson-White syndrome

* A narrow complex tachycardia with an accessory conduction pathway, often termed " supraventricular tachycardia with pre-excitation " ( e. g. Wolff-Parkinson-White syndrome ).

* Genetics Home Reference: Wolff-Parkinson-White syndrome ( United States National Library of Medicine, Bethesda, Maryland )

* Wolff-Parkinson-White syndrome

In one case reported in Poland in 1998, an 18-year-old man developed Wolff-Parkinson-White syndrome, arrhythmia, and suffered myocardial infarction after ingesting P. semilanceata frequently over the period of a month.

* Wolff-Parkinson-White syndrome

However, in individuals with a pre-existing accessory conduction pathway, such as the bundle of Kent in Wolff-Parkinson-White syndrome, the accessory pathway may conduct activity from the atria to the ventricles at a rate that the AV node would usually block.

Flecainide is used in the treatment of many types of supraventricular tachycardias, including AV nodal re-entrant tachycardia ( AVNRT ) and Wolff-Parkinson-White syndrome ( WPW ).

* AV reciprocating tachycardia ( AVRT )-visible or concealed ( including Wolff-Parkinson-White syndrome )

Wolff-Parkinson-White syndrome is a relatively common abnormality with an accessory pathway, the Bundle of Kent crossing the AV valvular ring.

* Wolff-Parkinson-White syndrome

The fast and slow pathways should not be confused with the accessory pathways that give rise to Wolff-Parkinson-White syndrome ( WPW syndrome ) or atrioventricular reciprocating tachycardia ( AVRT ).

All these ECG-based technologies also enable the distinction between AVNRT and other tachycardias such as atrial fibrillation, atrial flutter, sinus tachycardia, ventricular tachycardia and tachyarrhythmias related to Wolff-Parkinson-White syndrome, all of which may have symptoms that are similar to AVNRT.

* Wolff-Parkinson-White syndrome

* Wolff-Parkinson-White syndrome often accompanies

There is an enlargement of the aorta, which may cause an increased risk of abnormality in infants of women taking lithium during the first trimester of pregnancy ( though some have questioned this ) and in those with Wolff-Parkinson-White syndrome.

About 50 % of individuals with Ebstein anomaly have evidence of Wolff-Parkinson-White syndrome, secondary to the atrialized right ventricular tissue.

It can also be used to treat Wolff-Parkinson-White syndrome by prolonging the refractory period of the accessory pathway.

Louis Wolff and John Parkinson, who together described the Wolff-Parkinson-White syndrome, a condition of uncontrolled rapid heartbeat.

Hodson suffered from Wolff-Parkinson-White syndrome ( rapid heart beat ) during his time in the NHL, and affectionately earned the nickname " Ticker " from teammates.

Catheter ablation is an invasive procedure used to remove a faulty electrical pathway from the hearts of those who are prone to developing cardiac arrhythmias such as atrial fibrillation, atrial flutter, supraventricular tachycardias ( SVT ) and Wolff-Parkinson-White syndrome.

Wolff-Parkinson-White Syndrome is a combination of SVT with characteristic findings on ECG.

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.

This syndrome may be hard to recognize, as it starts several days after delivery, for example, as late as 21 day for chlordiazepoxide.

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.