| knee joint | A compound condylar synovial joint consisting of the joint between the condyles of the femur and the condyles of the tibia, articular menisci (semilunar cartilages) being interposed, and the articulation between femur and patella. Synonym: articulatio genus. (05 Mar 2000) |
|---|---|
| femoropatellar joint | The articulation of the facets on the articular surface of the patella with corresponding surfaces on the femoral condyles. (05 Mar 2000) |
| fibrous joint | A union of two bones by fibrous tissue such that there is no joint cavity and almost no motion possible; the types of fibrous joints are sutures, syndesmoses, and gomphoses. Synonym: articulatio fibrosa, immovable joint, junctura fibrosa, synarthrodia, synarthrodial joint. (05 Mar 2000) |
| flail joint | A joint with loss of function caused by loss of ability to stabilise the joint in any plane within its normal range of motion. (05 Mar 2000) |
| lateral atlantoaxial joint | A condylar synovial joint between the inferior articular facets of the atlas and the superior articular facets of the axis. Synonym: articulatio atlantoaxialis lateralis, lateral atlantoepistrophic joint. (05 Mar 2000) |
| lateral atlantoepistrophic joint | A condylar synovial joint between the inferior articular facets of the atlas and the superior articular facets of the axis. Synonym: articulatio atlantoaxialis lateralis, lateral atlantoepistrophic joint. (05 Mar 2000) |
| lateral ligament of temporomandibular joint | <anatomy> The capsular ligament that passes obliquely down and backward across the lateral surface of the temporomandibular joint. Synonym: ligamentum laterale articulationis temporomandibularis, Ferrein's ligament, lateral ligament of temporomandibular joint, ligamentum temporomandibulare, temporomandibular ligament. (05 Mar 2000) |
| lumbosacral joint | The articulation of the fifth lumbar vertebra with the sacrum. Synonym: articulatio lumbosacralis, junctura lumbosacralis. (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) |
| Achard-Thiers syndrome | <syndrome> One form of a virilizing disorder of adrenocortical origin in women, characterised by masculinization and menstrual disorders in association with manifestations of diabetes mellitus, such as glucosuria. (05 Mar 2000) |
| Achenbach syndrome | <syndrome> Haematoma of the finger pad with accompanying oedema; of unknown cause in the absence of disturbances in blood coagulation mechanisms. (05 Mar 2000) |