| total or partial anomalous pulmonary venous connections | Connections in which some or all of the pulmonary veins connect to the right atrium or one of its tributaries. (05 Mar 2000) |
|---|---|
| Trusler's rule for pulmonary artery banding | A method that gives guidance as to the correct tightness of the band; the degree of banding for a complex congenital cardiac anomaly with bidirectional shunting less than that for simple ones. (05 Mar 2000) |
| tuberculosis, pulmonary | Tuberculosis of the lungs. (12 Dec 1998) |
| juxta-oesophageal pulmonary lymph nodes | Several nodes of the posterior mediastinal group located along either side of the oesophagus; they receive lymph from both the oesophagus and the lungs. Synonym: nodi lymphatici juxta-oesophageales pulmonales. (05 Mar 2000) |
| left inferior pulmonary vein | <anatomy, vein> The vein returning oxygenated blood from the inferior lobe of the left lung to the left atrium. Synonym: vena pulmonalis inferior sinistra. (05 Mar 2000) |
| left pulmonary artery | <anatomy, artery> The shorter of the two terminal branches of the pulmonary trunk, it pierces the pericardium to enter the hilum of the left lung. Its branches accompany the segmental and subsegmental bronchi. Branches to the superior lobe (rami lobi superioris ) are apical (ramus apicalis ), anterior ascending (ramus anterior ascendens ), anterior descending (ramus anterior descendens ), posterior (ramus posterior ), and lingular (ramus lingularis ), the last having inferior and superior branches (rami lingulares inferior et superior ). Branches to the inferior lobe (rami lobi inferioris ) are the superior branch of the inferior lobe (ramus superior lobi inferior ) and the medial (medialis), anterior, lateral (lateralis) and posterior basal branches (rami basalis ). Synonym: arteria pulmonalis sinistra. (05 Mar 2000) |
| left superior pulmonary vein | The vein returning oxygenated blood from the left superior lobe of the lung to the left atrium. Synonym: vena pulmonalis superior sinistra. (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) |
| achoo syndrome | <syndrome> A disorder characterised by nearly uncontrollable paroxysms of sneezing provoked in a reflex fashion by the sudden exposure of a dark-adapted subject to intensely bright light, usually sunlight. Inheritance: autosomal dominant. (05 Aug 1998) |