| syndrome of approximate relevant answers | <syndrome> A psychotic-like condition, without the symptoms and signs of a traditional psychosis, occurring typically in prisoners who feign insanity; e.g., such a person, when asked to multiply 6 by 4, will give 23 as the answer, or he will call a key a lock. See: malingering, factitious disorder. Synonym: nonsense syndrome, syndrome of approximate relevant answers, syndrome of deviously relevant answers. (05 Mar 2000) |
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| syndrome of deviously relevant answers | <syndrome> A psychotic-like condition, without the symptoms and signs of a traditional psychosis, occurring typically in prisoners who feign insanity; e.g., such a person, when asked to multiply 6 by 4, will give 23 as the answer, or he will call a key a lock. See: malingering, factitious disorder. Synonym: nonsense syndrome, syndrome of approximate relevant answers, syndrome of deviously relevant answers. (05 Mar 2000) |
| Syndrome of Inappropriate ADH | <endocrinology, syndrome> Inappropriate antidiuretic hormone secretion produces a disorder of fluid and electrolyte balance which results in the inability to excrete dilute urine. Inappropriate antidiuretic hormone secretion is seen in association with certain cancers (for example oat cell lung cancer, pancreatic, prostate, Hodgkin's disease), central nervous system disorders, head injury, myxoedema, psychosis and certain drugs. Symptoms include weight gain, nausea, vomiting, muscle cramps, confusion and convulsions. Incidence: approximately 1 in 100,000. Acronym: SIADH (18 Nov 1997) |
| syndrome of inappropriate secretion of antidiuretic hormone | Continued secretion of antidiuretic hormone despite low serum osmolality and expanded extracellular volume. (05 Mar 2000) |
| syndrome premenstrual | A combination of emotional, physical, psychological, and mood disturbances that occur after ovulation and normally end with the onset of the menstrual flow. (12 Dec 1998) |
| syndrome x | Angina pectoris or angina-like chest pain with a normal coronary arteriogram and positive exercise test. The cause of the syndrome is unknown. While its recognition is of clinical importance, its prognosis is excellent. (12 Dec 1998) |
| syndrome, antiphospholipid antibody | An immune disorder characterised by the presence of abnormal antibodies in the blood associated with certain medical conditions including abnormal blood clotting, migraine headaches, premature miscarriage, and low blood platelet counts (thrombocytopenia). (12 Dec 1998) |
| syndrome, barlow's | Barlow's syndrome is mitral valve prolapse (also known as click murmur syndrome ), the most common heart valve abnormality, affecting 5-10% of the world population. Most patients have no symptoms and require no treatment. However, the condition can be associated with fatigue and/or palpitations. The mitral valve prolapse can often be detected by a doctor during examination of the heart and can be confirmed with an echocardiogram. Patients are usually given antibiotics prior to any procedure which might introduce bacteria into the bloodstream, including dental work and minor surgery. (12 Dec 1998) |
| syndrome, behcet's | Behcet's syndrome is classically characterised as a triad of symptoms that include recurring crops of mouth ulcers (called apthous ulcers), genital ulcers, and inflammation of a specialised area around the pupil of the eye, the uvea. (the inflammation is called uveitis.) the cause of behcet's syndrome is not known. The disease is more frequent and severe in patients from the eastern mediterranean and asia than those of european descent. (12 Dec 1998) |
| syndrome, bernard | A complex of abnormal findings, namely sinking in of one eyeball, ipsilateral ptosis (drooping of the upper eyelid on the same side) and miosis (constriction of the pupil of that eye) together with anhidosis (lack of sweating) and flushing of the affected side of the face. Due to paralysis of certain nerves (specifically, the cervical sympathetic nerves). Also called horner-bernard syndrome, bernard-horner syndrome and horner's ptosis but best known today as horner syndrome. (12 Dec 1998) |
| syndrome, bloch-sulzberger | Also known as incontinentia pigmenti (ip). A genetic disease with blisters that develop soon after birth on the trunk and limbs, then heal, but leave dark (hyperpigmented) streaks and marble-like whorls on the skin. (the name came from the erroneous idea that the skin cells were incontinent of pigment and could not contain it normally.) other key features of ip include dental and nail abnormalities, bald patches, and (in about 1/3rd of cases) mental retardation. Ip is an x-linked dominant with male lethality. The ip gene is in band q28 on the x chromosome. Mothers with ip have an equal chance of having a normal or ip daughter or a normal son. The ip sons die before birth. Ip is also known as bloch-sulzberger syndrome. (12 Dec 1998) |
| syndrome, brown's | An ophthalmology (eye) problem. Brown's syndrome presents at birth (congenitally) and is characterised by an inability to elevate the eyeball when also trying to move the eyeball to the outside. (12 Dec 1998) |
| syndrome, conn's | Overproduction of the hormone aldosterone from a tumour containing tissue like that in the outer portion (cortex) of the adrenal gland. Excess aldosterone (pronounced al-do-ster-one) results in low potassium levels (hypokalaemia), underacidity of the body (alkalosis), muscle weakness, excess thirst (polydipsia), excess urination (polyuria), and high blood pressure (hypertension). Also called primary aldosteronism and hyperaldosteronism. Named after the american physician jerome w. Conn. (12 Dec 1998) |
| syndrome, cracked tooth | A toothache caused by a broken tooth (tooth fracture) without associated cavity or advanced gum disease. Biting on the area of tooth fracture can cause severe sharp pains. These fractures are usually due to chewing or biting hard objects such as hard candies, pencils, nuts, etc. Sometimes, the fracture can be seen by painting a special dye on the cracked tooth. Treatment usually is to protect the tooth with a crown. However, if placing a crown does not relieve pain symptoms, a root canal procedure may be necessary. (12 Dec 1998) |
| syndrome, creutzfeldt-jakob | Better known as creutzfeldt-jakob disease (cjd). A dementing disease of the brain. It is believed due to an unconventional (not a bacteria or virus), transmissible agent called a prion. Symptoms of cjd include forgetfulness, nervousness, jerky trembling hand movements, unsteady gait, muscle spasms, chronic dementia, balance disorder, and loss of facial expression. Cjd is classified as a spongiform encephalopathy. most cases occur randomly (sporadically), but inherited forms exist. There is neither treatment nor cure for cjd. Other names for cjd include jakob-creutzfeldt disease and spastic pseuodoparalysis. (12 Dec 1998) |
| syndrome X |
A cluster of risk factors that together, put someone at higher risk of coronary artery disease. These risk factors include: central obesity (excessive fat tissue in the abdominal region), glucose intolerance, high triglycerides and low HDL cholesterol, and high blood pressure (http://www.americanheart.org)
출처: www.clevelandclinic.org/heartcenter/pub/glossary/s...
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| syndrome |
A complex of various disease symptoms.
출처: depts.washington.edu/registry/glossary.htm
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| syndactyly |
a congenital problem characterized by a union of fingers or toes.
출처: ymghealthinfo.org/content.asp
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| syndrome |
a group of characteristics that occur together.
출처: ymghealthinfo.org/content.asp
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| syndrome |
a set of symptoms that occur together
출처: www.southalabama.edu/alliedhealth/cls/Ravine/gloss...
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