| TI | inversion time; temporal integration; terminal ileum; thalassemia intermedia; therapeutic index; tho... |
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| TL | temporal lobe; terminal limen; thermolabile; thermoluminescence; threat to life; thymus-leukemia [an... |
| TLE | temporal lobe epilepsy; thin-layer electrophoresis; total lipid extract |
| TP | temperature and pressure; temperature probe; temporal peak; temporoparietal; tension pneumothorax; t... |
| AAS | Aarskog-Scott [syndrome]; acid aspiration syndrome; alcoholic abstinence syndrome; American Academy ... |
| epilepsy, temporal lobe | Epileptic seizures characterised by simple partial seizures, complex partial seizures, and secondary generalised seizures, or combinations of these. Seizures may present with autonomic and/or psychic symptoms and certain sensory phenomena such as olfactory and auditory. most common is an epigastric rising sensation. Some seizures may begin with motor arrest and continue with oro-alimentary automatisms (with other automatisms following). Attacks are followed by amnesia and recovery is gradual. Usually, there is a history of febrile seizures in the individual or a history of seizures in the family. Seizures occur in clusters, randomly, or at intervals. (12 Dec 1998) |
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| tympanic part of temporal bone | The bony plate forming the greater part of the anterior wall of the bony part of the external acoustic meatus and the tympanic cavity and the posterior wall of the mandibular fossa. Synonym: pars tympanica ossis temporalis, tympanic part of temporal bone. (05 Mar 2000) |
| tympanic plate of temporal bone | The bony plate forming the greater part of the anterior wall of the bony part of the external acoustic meatus and the tympanic cavity and the posterior wall of the mandibular fossa. Synonym: pars tympanica ossis temporalis, tympanic part of temporal bone. (05 Mar 2000) |
| jugular notch of temporal bone | The notch in the temporal bone which forms one boundary of the jugular foramen. Synonym: incisura jugularis ossis temporalis. (05 Mar 2000) |
| zygomatic process of temporal bone | The anterior process of the temporal bone that articulates with the temporal process of the zygomatic bone to form the zygomatic arch. Synonym: processus zygomaticus ossis temporalis. (05 Mar 2000) |
| first temporal convolution | A longitudinal gyrus on the lateral surface of the temporal lobe between the lateral (sylvian) fissure and the superior temporal sulcus. Synonym: gyrus temporalis superior, first temporal convolution, superior temporal convolution. (05 Mar 2000) |
| frontal branch of superficial temporal artery | <anatomy, artery> Terminal branch of superficial temporal artery (with parietal branch) supplying anterolateral scalp and underlying musculature, periosteum, and outer table of cranium; anastomosis: across midline with contralateral partner; supratrochlear and supraorbital arteries. Synonym: ramus frontalis arteriae temporalis superficialis. (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) |