| PLS | Papillon-Lefevre syndrome; polydactyly-luxation syndrome; preleukemic syndrome; primary lateral scle... |
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| PMS | patient management system; perimenstrual syndrome; periodic movements during sleep; phenazine methos... |
| PS | pacemaker syndrome; paired stimulation; paradoxical sleep; paraspinal; parasympathetic; Parkinson sy... |
| SS | disulfide; sacrosciatic; saline soak; saline solution; saliva sample; saliva substitute; Salmonella-... |
| SSS | scalded skin syndrome; secondary Sjogren syndrome; sick sinus syndrome; specific soluble substance; ... |
| transverse cervical veins | Venae comitantes of the corresponding arteries, emptying into the external jugular vein or sometimes into the subclavian vein. Synonym: venae transversae colli, transverse veins of neck. (05 Mar 2000) |
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| unstable cervical spine fractures | <radiology> Flexion: bilateral interfacetal dislocation, flexion teardrop fracture (usually C5 or C6) extension: extension teardrop fracture (usually C2 or C3), hangman's fracture, extension-dislocation, extension-fracture-dislocation, odontoid fracture vertical compression: Jefferson burst fracture see: cervical spine fractures (12 Dec 1998) |
| laryngopharyngeal branches of superior cervical ganglion | Branches conveying postganglionic sympathetic fibres from the superior cervical ganglion to the pharyngeal plexus. Synonym: rami laryngopharyngei ganglii cervicalis superioris. (05 Mar 2000) |
| lateral cervical nuclei | Diffusely arranged nucleus located in the dorsal portions of the lateral funiculus in about cervical levels C1-C3; synaptic station for the spinocervicothalamic tract. (05 Mar 2000) |
| lateral deep cervical lymph nodes | The lymph nodes located in the posterior triangle of the neck beneath the deep cervical fascia; they empty into the jugular trunk on the right or left side; the group is subdivided into four smaller chains: anterior jugular lymph nodes, lateral jugular lymph nodes, accessory nerve lymph nodes, and supraclavicular lymph nodes. Synonym: nodi lymphatici cervicales laterales profundi. (05 Mar 2000) |
| lateral part of posterior cervical intertransversarii muscles | lateral part of posterior cervical intertransversarii muscles |
| lateral superficial cervical lymph nodes | One to four nodes lying along the external jugular vein; they drain the skin and superficial structures over the region of the sternocleidomastoid muscle and send efferent vessels to the deep lateral cervical lymph nodes. Synonym: nodi lymphatici cervicales laterales superficiales. (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) |