| ID50 | median infective dose |
|---|---|
| LC50 | median lethal concentration |
| LD50 | median lethal dose |
| LM | lactic acid mineral [medium]; lactose malabsorption; laryngeal mask; laryngeal muscle; lateral malle... |
| MCF | macrophage chemotactic factor; median cleft face; medium corpuscular fragility; microcomplement fixa... |
| sensory paralysis | Loss of sensation; anaesthesia. (05 Mar 2000) |
|---|---|
| hyperkalaemic periodic paralysis | A form of periodic paralysis in which the serum potassium level is elevated during attacks; onset occurs in infancy, attacks are frequent but relatively mild, and myotonia is often present; autosomal dominant inheritance. (05 Mar 2000) |
| hypokalaemic periodic paralysis | <biochemistry> A rare inherited disorder, affecting men more often than women, characterised by intermittent episodes of muscle weakness or paralysis. One form, known as hypokalaemic periodic paralysis, is an autosomal recessive disorder that is characterised by bouts of muscle weakness (or paralysis) accompanied by low serum potassium levels. Inheritance: autosomal recessive. Incidence: 1 in 100,000. (11 Jan 1998) |
| sleep paralysis | <neurology, physiology> A condition that occurs in REM stage sleep. There is no movement of the skeletal muscles in this stage of sleep. See: REM stage sleep. (27 Sep 1997) |
| hysterical paralysis | A psychosomatic numbness of a limb sometimes to the point of paralysis. See: hysteria. (05 Mar 2000) |
| sodium-responsive periodic paralysis | A form of periodic paralysis in which the serum potassium level is within normal limits during attacks; onset usually occurs between the ages of 2 and 5 years; there is often severe quadriplegia, usually improved by the administration of sodium salts; autosomal dominant inheritance. Synonym: sodium-responsive periodic paralysis. (05 Mar 2000) |
| spastic spinal paralysis | A type of cerebral palsy in which there is bilateral spasticity, with the lower extremities more severely affected. Compare: flaccid paralysis. Synonym: Erb-Charcot disease, infantile diplegia, Little's disease, spastic spinal paralysis, tabes spasmodica. (05 Mar 2000) |
| spinal paralysis | Loss of motor power due to a lesion of the spinal cord. Synonym: myeloparalysis, myeloplegia, rachioplegia. (05 Mar 2000) |
| normokalaemic periodic paralysis | A form of periodic paralysis in which the serum potassium level is within normal limits during attacks; onset usually occurs between the ages of 2 and 5 years; there is often severe quadriplegia, usually improved by the administration of sodium salts; autosomal dominant inheritance. Synonym: sodium-responsive periodic paralysis. (05 Mar 2000) |
| supranuclear paralysis | Paralysis due to lesions above the primary motor neurons. (05 Mar 2000) |
| diphtheritic paralysis | <otolaryngology> Paralysis affecting the uvula most frequently, but also any other muscle, due to toxic neuritis; usually appears in the second or third week following the beginning of the attack of diphtheria. Synonym: diphtheritic paralysis. (05 Mar 2000) |
| diver's paralysis | Lay term for decompression sickness. (05 Mar 2000) |
| Duchenne-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) |
| immune paralysis | The induction of tolerance in mice due to injection of large amounts of polysaccharide. The polysaccharide is poorly metabolised and the paralysis remains only during the persistence of the above. (05 Mar 2000) |
| immunological paralysis | Lack of specific antibody production after exposure to large doses of the antigen; immunological paralysis disappears when the antigen is eliminated. See: immunologic tolerance. (05 Mar 2000) |