| PIP | paralytic infantile paralysis; peak inflation pressure, peak inspiratory pressure; periodic interim ... |
|---|---|
| SCARF | skeletal abnormalities, cutis laxa, craniostenosis, psychomotor retardation, facial abnormalities [s... |
| short-FRAME | short stature-facial anomalies-Rieger anomaly-midline anomalies-enamel defects [syndrome] |
| VCFS | velo-cardio-facial syndrome |
| CN | Cranial Nerve |
| 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) |
| familial periodic paralysis | <neurology> 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. (27 Sep 1997) |
| 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) |
| anterior facial vein | <anatomy, vein> A continuation of the angular vein at the medial angle of the eye. It passes diagonally downward and outward, joining with the retromandibular vein below the border of the lower jaw before emptying into the internal jugular vein. Synonym: anterior facial vein, vena facialis anterior, vena facialis. (05 Mar 2000) |
| atypical facial neuralgia | Periodic pain in any region of the face, teeth, tongue, and occasionally in the occipital or shoulder area, which lasts several minutes to several days but has no trigger point and lacks the paroxysmal character of tic douloureux. Synonym: atypical facial neuralgia. (05 Mar 2000) |
| Broca's facial angle | The angle formed by the intersection at the biauricular axis of lines drawn from the supraorbital point and the alveolar point. Synonym: Broca's angles. (05 Mar 2000) |
| velo-cardio-facial syndrome | <syndrome> Also known as shprintzen syndrome, this more than is a congenital malformation (birth defect) syndrome with cleft palate, heart defect, abnormal face, and learning problems. The condition is therefore called the velo-cardio-facial (vcf) syndrome. (the velum is the soft palate). Other less frequent features include short stature, small-than-normal head (microcephaly), mental retardation, minor ear anomalies, slender hands and digits, and inguinal hernia. The cause is usually a microdeletion in chromosome band 22q11.2, just as in digeorge syndrome. Vcf and digeorge syndromes are different clinical expressions of essentially the same chromosome defect. Of essentially the same chromosome defect. (12 Dec 1998) |