| FMTC | Familial Medullary Thyroid Carcinoma |
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| FPC | Familial ; °¡Á·¼º ¿ëÁ¾¼º ÁõÈıº |
| HSM Syndrome | juvenile-familial Endocrinopathy Hypoparathyroidism Addison's Disease Menillansis |
| AFI | amaurotic familial idiocy |
| AREPA | acetazolamide-responsive familial paroxysmal ataxia |
| Erb paralysis | A type of brachial birth palsy in which there is paralysis of the muscles of the upper arm and shoulder girdle (deltoid, biceps, brachialis, and brachioradialis muscles) due to a lesion of the upper trunk of the brachial plexus or of the roots of the fifth and sixth cervical roots. Synonym: Duchenne-Erb paralysis, Erb paralysis. (05 Mar 2000) |
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| Erb spinal paralysis | Chronic myelitis of syphilitic origin. (05 Mar 2000) |
| jake paralysis | Neuropathy produced by drinking synthetic Jamaican ginger (or "jake" in the vernacular) containing triorthocresylphosphate. Synonym: ginger paralysis. (05 Mar 2000) |
| facial paralysis | Paralysis of the facial muscles, usually unilateral, due to either a lesion involving the nucleus or the facial nerve peripheral to the nucleus (peripheral facial paralysis) or a supranuclear lesion in the cerebrum or upper brainstem (central facial paralysis). With latter, facial weakness is usually partial and the upper portion of the face is relatively spared, due to bilateral cortical connections. (12 Dec 1998) |
| Zenker's paralysis | Paresthesia and paralysis in the area of the external popliteal nerve. (05 Mar 2000) |
| faucial paralysis | Paralysis of the velum pendulum palati and the muscles forming the anterior pillars of the fauces. Synonym: faucial paralysis, isthmoplegia. Origin: G. Isthmos, isthmus, + paralysis (05 Mar 2000) |
| Klumpke's paralysis | A type of brachial birth palsy in which there is paralysis of the muscles of the distal forearm and hand (all ulnar innervated muscles, plus more distal radial and median-innervated muscles), due to a lesion of the lower trunk of the brachial plexus, or of the C8 and T1 cervical roots. Synonym: Dejerine-Klumpke palsy, Dejerine-Klumpke syndrome, Klumpke's paralysis. (05 Mar 2000) |
| flaccid paralysis | Paralysis with a loss of muscle tone. Compare: spastic diplegia. (05 Mar 2000) |
| lambing paralysis | A highly fatal metabolic disease of well-nourished ewes in the late stages of pregnancy, especially in ewes carrying twin lambs; it is caused by carbohydrate depletion of the blood and tissues, and is characterised by hypoglycaemia, ketonuria, fatty infiltration of the liver, rapid emaciation, coma, and a high death rate. Synonym: lambing paralysis, lambing sickness. (05 Mar 2000) |
| Landry's paralysis | <neurology, syndrome> Acute infective polyneuritis that results in a form of peripheral neuropathy with temporary loss of movement and sensation due to inflammation of multiple nerves and loss of myelin. The exact cause is unknown but has been associated with an abnormal immune response to viral infection, particularly cytomegalovirus infection, in which there is cell-mediated immunity to a component of myelin. The disease may be autoimmune in origin and complete recovery can take up to six months. Synonym: Guillain-Barre syndrome (12 Jul 2000) |
| fowl paralysis | See: avian lymphomatosis. (05 Mar 2000) |
| lead paralysis | Paralysis of the extensor muscles of the wrist causing wrist-drop; occurs in lead poisoning. Synonym: lead paralysis. (05 Mar 2000) |
| benign familial chorea | A rare, nonprogressive movement disorder characterised by chorea and athetosis appearing in early childhood, most commonly manifested as gait ataxia and upper limb coordination. Intellect is unaffected. Probably autosomal-dominance inheritance with incomplete penetrance. (05 Mar 2000) |
| benign familial chronic pemphigus | Recurrent eruption of vesicles and bullae that become scaling and crusted lesions with vesicular borders, predominantly of the neck, groin, and axillary regions; autosomal dominant inheritance, presenting in late adolescence or early adult life. Synonym: Hailey-Hailey disease. (05 Mar 2000) |
| benign familial icterus | Mild jaundice due to increased amounts of unconjugated bilirubin in the plasma without evidence of liver damage, biliary obstruction, or haemolysis; thought to be due to an inborn error of metabolism in which the excretion of bilirubin by the liver is defective, ascribed to decreased conjugation of bilirubin as a glucuronide or impaired uptake of hepatic bilirubin. Synonym: benign familial icterus, constitutional hepatic dysfunction, Gilbert's disease, Gilbert's syndrome, Hebra's disease. (05 Mar 2000) |
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