| HS | Haber syndrome; half strength; hamstring; hand surgery; Hartmann solution; head sling; healthy subje... |
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| KS | Kallmann syndrome; Kaposi sarcoma; Kartagener syndrome; Kawasaki syndrome; keratan sulfate; ketoster... |
| RS | radioscaphoid; random sample; rating schedule; Raynaud syndrome; recipient's serum; rectal sinus; re... |
| AAS | Aarskog-Scott [syndrome]; acid aspiration syndrome; alcoholic abstinence syndrome; American Academy ... |
| ABS | abdominal surgery; acute brain syndrome; Adaptive Behavior Scale; admitting blood sugar; adult bovin... |
| Erb spinal paralysis | Chronic myelitis of syphilitic origin. (05 Mar 2000) |
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| 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) |
| 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) |
| Aarskog-Scott syndrome | A syndrome of ocular hypertelorism, anteverted nostrils, broad upper lip, saddle-bag scrotum, and laxity of ligaments resulting in genu recurvatum, flat feet, and hyperextensible fingers; X-linked and autosomal dominant forms. Synonym: Aarskog-Scott syndrome. (05 Mar 2000) |
| Aarskog syndrome | <syndrome> Grier et al. (1983) reported father and 2 sons with typical Aarskog syndrome, including short stature, hypertelorism, and shawl scrotum. They tabulated the findings in 82 previous cases. X-linked recessive inheritance has been repeatedly suggested. The family reported by Welch (1974) had affected males in 3 consecutive generations. Thus, there is either genetic heterogeneity or this is an autosomal dominant with strong sex-influence and possibly ascertainment bias resulting from use of the shawl scrotum as a main criterion. Stretchable skin was present in the cases of Grier et al. (1983). Teebi et al. (1993) reported the case of an affected mother and 4 sons (including a pair of monozygotic twins) by 2 different husbands. They suggested that the manifestations were as severe in the mother as in the sons and that this suggested autosomal dominant inheritance. Actually, the mother seemed less severely affected, compatible with X-linked inheritance. Clinical signs: Mild to moderate short stature,normocephaly, Widow's peak hair, maxillary hypoplasia, broad nasal bridge, anteverted nostrils, long philtrum, broad upper lip, curved linear dimple below the lower lip, hypertelorism, ptosis, down-slanted palpebral fissures, ophthalmoplegia, strabismus, hyperopic astigmatism, large cornea, floppy ears, lop-ears,cleft lip/palate, shawl scrotum, saddle-bag scrotum, cryptorchidism, brachydactyly, digital contractures, clinodactyly, mild syndactyly, transverse palmar crease, lymphoedema of the feet, ligamentous laxity, osteochondritis dissecans, proximal finger joint hyperextensibility, flexed distal finger joints, genu recurvatum, flat feet, stretchable skin, cervical spine hypermobility, odontoid anomaly, macrocytic anaemia, hemochromatosis, hepatomegaly, portal cirrhosis, imperforate anus, rectoperineal fistula, interstitial pulmonary disease, sternal deformity. Inheritance: Sex-influenced autosomal dominant form, also X-linked form. (05 Aug 1998) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |