| papillary stasis | An obsolete term for papilledema. (05 Mar 2000) |
|---|---|
| venous stasis | Congestion and slowing of circulation in veins due to blockage by either obstruction or high pressure in the venous system, usually best seen in the feet and legs. (05 Mar 2000) |
| venous-stasis retinopathy | A uniocular retinopathy associated with occlusion of the central retinal vein; a nonischemic central retinal vein occlusion. (05 Mar 2000) |
| pressure stasis | Cyanotic asphyxia due to trauma; the extravasation of blood into the skin and conjunctivae, produced by a sudden mechanical increase in venous pressure, analogous to the Rumpel-Leede test; it is common in those who have been hanged, and is seen occasionally in crush injuries. Synonym: pressure stasis. (05 Mar 2000) |
| stasis | A word termination indicating the maintenance of (or maintaining) a constant level, preventing increase or multiplication. Origin: Gr. = a standing still (18 Nov 1997) |
| stasis cirrhosis | An extensive fibrotic reaction within the liver as a result of chronic constrictive pericarditis or prolonged congestive heart failure; true cirrhosis with fibrous bridging of lobules is unusual. Synonym: cardiac liver, congestive cirrhosis, pseudocirrhosis, stasis cirrhosis. (05 Mar 2000) |
| stasis dermatitis | Erythema and scaling of the lower extremities due to impaired venous circulation, seen commonly in older women or secondary to deep vein thrombosis. (05 Mar 2000) |
| stasis eczema | Eczematous eruption on legs due to or aggravated by vascular stasis. (05 Mar 2000) |
| stasis ulcer | Ulcer due to varicose veins. Chronic venous insufficiency in the deep veins of the legs leads to shunting the venous return into the superficial veins, in which pressure and flow rate, as well as oxygen content, are increased. (12 Dec 1998) |
| intestinal stasis | Intestinal stasis; a retardation or arrest of the passage of the intestinal contents. Synonym: intestinal stasis. Origin: entero-+ G. Stasis, a standing (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) |
| abstinence syndrome | <syndrome> A constellation of physiologic changes undergone by persons or animals who have become physically dependent on a drug or chemical due to prolonged use at elevated doses, but who are abruptly deprived of that substance. The abstinence syndrome varies with the drug to which dependence has developed. Generally the effects observed are in an opposite direction from those produced by the drug; e.g., the withdrawal syndrome from central nervous system depressants such as barbiturates and benzodiazepines consists of insomnia, restlessness, tremulousness, hallucinations, and, in the extreme, tonic-clonic convulsions which may prove fatal. The onset time and severity of the abstinence syndrome depend upon how rapidly the drug disappears from the body. (05 Mar 2000) |
| Achard syndrome | <syndrome> Arachnodactyly with small receding mandible, broad skull, and joint laxity limited to the hands and feet; genetics unclear. (05 Mar 2000) |