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Что (кто) такое firehose syndrome - определение

SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS

Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; Reye’s syndrome

Найдено результатов: 2420

firehose syndrome

<networking, jargon> An absence, failure or inadequacy of flow control mechanisms causing the sender to overwhelm the receiver. The implication is that, like trying to drink from a firehose, the consequenses are worse than just loss of data, e.g. the receiver may crash. See ping-flood. [Jargon File] (2007-03-12)

Reye's syndrome

['re?z, 'r??z]

¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.

Origin

1960s: named after the Australian paediatrician Ralph D. K. Reye.

Frey's syndrome

HUMAN DISEASE

Auriculotemporal syndrome; Frey syndrome

Frey's syndrome (also known as Baillarger's syndrome, Dupuy's syndrome, auriculotemporal syndrome, or Frey-Baillarger syndrome) is a rare neurological disorder resulting from damage to or near the parotid glands responsible for making saliva, and from damage to the auriculotemporal nerve often from surgery.

https://en.wikipedia.org/wiki/Frey's_syndrome

Metabolic syndrome

DISEASE DIAGNOSED BY A CLUSTER OF AT LEAST 3 OUT OF THE FOLLOWING CONDITIONS: ABDOMINAL OBESITY, HIGH BLOOD PRESSURE, HIGH BLOOD SUGAR, HIGH SERUM TRIGLYCERIDES, LOW SERUM HIGH-DENSITY LIPOPROTEIN

Metabolic syndrome X; Dysmetabolic syndrome; Syndrome X (metabolic); Metabolic syndrome x; Insulin Resistance Syndrome; Metabolic Syndrome; Metabolic Syndrome X; Metabolic dysfunction; Metabolic syndromes; Draft:Cardiometabolic syndrome

Metabolic syndrome is a clustering of at least three of the following five medical conditions: abdominal obesity, high blood pressure, high blood sugar, high serum triglycerides, and low serum high-density lipoprotein (HDL).

https://en.wikipedia.org/wiki/Metabolic_syndrome

Meigs's syndrome

CHARACTERIZED BY PLEURAL EFFUSION, ASCITES AND NON-MALIGNANT OVARIAN NEOPLASM

Meig's syndrome; Meigs syndrome; Meigs' syndrome

In medicine, Meigs's syndrome, also Meigs syndrome or Demons–Meigs syndrome, is the triad of ascites, pleural effusion, and benign ovarian tumor (ovarian fibroma, fibrothecoma, Brenner tumour, and occasionally granulosa cell tumour). Meigs syndrome resolves after the resection of the tumor.

https://en.wikipedia.org/wiki/Meigs's_syndrome

Firehose (band)

BAND

FIREHOSE; LowFLOWs: The Columbia Anthology ('91-'93); LowFLOWs: The Columbia Anthology (’91-’93)

Firehose (stylized as fIREHOSE) was an American alternative rock band consisting of Mike Watt (bass, vocals), Ed Crawford (guitar, vocals), and George Hurley (drums). They were initially active from 1986 to 1994, and briefly reunited in 2012.

https://en.wikipedia.org/wiki/Firehose_(band)

Alström syndrome

RARE GENETIC DISORDER CAUSED BY MUTATIONS IN THE GENE ALMS1

Alstrom's syndrome; Alstroem syndrome; Alstrom syndrome; Alstrom Syndrome

Alström syndrome (AS), also called Alström–Hallgren syndrome, is a very rare autosomal recessive genetic disorder characterised by childhood obesity and multiple organ dysfunction. Symptoms include early-onset type 2 diabetes, cone-rod dystrophy resulting in blindness, sensorineural hearing loss and dilated cardiomyopathy.

https://en.wikipedia.org/wiki/Alström_syndrome

Stendhal syndrome

PSYCHOSOMATIC DISORDER

Stendhal's syndrome; Stendhal's Syndrome; Florence syndrome; Stendhal Syndrome; Stendal syndrome; Art panic attack; Stendal Syndrome

Stendhal syndrome, Stendhal's syndrome or Florence syndrome is a psychosomatic condition involving rapid heartbeat, fainting, confusion and even hallucinations, allegedly occurring when individuals become exposed to objects, artworks, or phenomena of great beauty and antiquity.

https://en.wikipedia.org/wiki/Stendhal_syndrome

Cockayne syndrome

RARE AND FATAL AUTOSOMAL RECESSIVE NEURODEGENERATIVE DISORDER

Cockayne's syndrome; Neiill-Dingwall syndrome; Neill-Dingwall syndrome; Dwarfism-retinal atrophy-deafness syndrome; Cockayne syndrome type 1; Cockayne syndrome type 2; Cockayne syndrome type 3; Cerebrooculofacioskeletal Syndrome; Cockayne Syndrome type II; COFS syndrome; Pena Shokeir II syndrome; Pena Shokeir syndrome type II; Cerebrooculofacioskeletal syndrome; Pena-Shokeir syndrome, type 2; Cockayne syndrome type A; Cockayne syndrome type B; Cockayne syndrome type C; Cockayne syndrome type III; Cerebro-oculo-facio-skeletal syndrome; Cerebrooculofacioskeletal syndrome 1; Cerebrooculofacioskeletal syndrome 2; Cerebrooculofacioskeletal syndrome 4; Cofs syndrome; Type II Cockayne syndrome; Pena-Shokeir syndrome type II; Cocaine Syndrome; Cocaine syndrome

Cockayne syndrome (CS), also called Neill-Dingwall syndrome, is a rare and fatal autosomal recessive neurodegenerative disorder characterized by growth failure, impaired development of the nervous system, abnormal sensitivity to sunlight (photosensitivity), eye disorders and premature aging.Bender M, Potocki L, Metry D.

https://en.wikipedia.org/wiki/Cockayne_syndrome

Mirizzi's syndrome

COMPLICATION OF CHOLELITHIASIS

Mirrizi's syndrome; Mirizzi syndrome; Mirizzis syndrome; Mirrizi’s syndrome

Mirizzi's syndrome is a rare complication in which a gallstone becomes impacted in the cystic duct or neck of the gallbladder causing compression of the common hepatic duct, resulting in obstruction and jaundice. The obstructive jaundice can be caused by direct extrinsic compression by the stone or from fibrosis caused by chronic cholecystitis (inflammation).

https://en.wikipedia.org/wiki/Mirizzi's_syndrome

Википедия

Reye syndrome

Reye syndrome is a rapidly worsening brain disease. Symptoms of Reye syndrome may include vomiting, personality changes, confusion, seizures, and loss of consciousness. While liver toxicity typically occurs in the syndrome, jaundice usually does not. Death occurs in 20–40% of those affected with Reye syndrome, and about a third of those who survive are left with a significant degree of brain damage.

The cause of Reye syndrome is unknown. It usually begins shortly after recovery from a viral infection, such as influenza or chickenpox. About 90% of cases in children are associated with aspirin (salicylate) use. Inborn errors of metabolism are also a risk factor. The syndrome is associated with changes on blood tests such as a high blood ammonia level, low blood sugar level, and prolonged prothrombin time. Often, the liver is enlarged in the syndrome.

Prevention is typically by avoiding the use of aspirin in children. When aspirin was withdrawn for use in children in the US and UK in the 1980s, a decrease of more than 90% in rates of Reye syndrome was seen. Early diagnosis of the syndrome improves outcomes. Treatment is supportive; mannitol may be used to help with the brain swelling.

The first detailed description of Reye syndrome was in 1963 by Australian pathologist Douglas Reye. The syndrome most commonly affects children. It affects fewer than one in a million children a year. The general recommendation to use aspirin in children was withdrawn because of Reye syndrome, with use only recommended in Kawasaki disease.

https://en.wikipedia.org/wiki/Reye syndrome