| VFD | Visual Field Defect |
|---|---|
| VSD | Ventricular Septal Defect ? Types of VSD 1. Subpulmonic(=... |
| APSD | aorticopulmonary septal defect |
| AVSD | atrioventricular septal defect |
| CSD | carotid sinus denervation; cat scratch disease; combined system disease; conditionally streptomycin ... |
chromate
| opening to cerebral aqueduct | Entrance to the cerebral aqueduct (of Sylvius) from the caudal part of the third ventricle. Synonym: aditus ad aqueductum cerebri, Bartholin's anus, opening to cerebral aqueduct. (05 Mar 2000) |
|---|---|
| toxoplasmosis, cerebral | Infection caused by the protozoan toxoplasma that presents itself in a subacute fashion with headache, focal neurologic signs, seizures, or altered mental status which can progress to coma. This condition is a commonly encountered opportunistic infection in aids patients. (12 Dec 1998) |
| extrapyramidal cerebral palsy | <neurology> A derangement marked by ceaseless occurrence of slow, sinuous, writhing movements, especially severe in the hands and performed involuntarily, it may occur after hemiplegia and is then known as posthemiplegic chorea. Synonym: mobile spasm. Origin: Gr. Athetos = not fixed (13 Nov 1997) |
| lateral cerebral fissure | The deepest and most prominent of the cortical fissures, extending from the anterior perforated substance first laterally at the deep incisure between the frontal and temporal lobes, then back and slightly upward over the lateral aspect of the cerebral hemisphere, with the superior temporal gyrus as its lower bank, the insula forming its greatly expanded floor. Two short side branches, the ramus anterior and ramus ascendens, divide the inferior frontal gyrus into an orbital part, triangular part, and opercular part. Synonym: sulcus lateralis cerebri, fissura cerebri lateralis, lateral cerebral fissure, sylvian fissure, fissure of Sylvius. (05 Mar 2000) |
| lateral cerebral fossa | The deep depression of the basal surface of the forebrain that corresponds in position to the anterior perforated substance. Bounded medially by the optic tract and rostrally by the orbital surface of the frontal lobe, it extends laterally around the overhanging pole of the temporal lobe into the Sylvian fissure (sulcus lateralis). Synonym: fossa lateralis cerebri, fossa of Sylvius, lateral fossa of brain, vallecula sylvii. (05 Mar 2000) |
| lateral cerebral sulcus | The deepest and most prominent of the cortical fissures, extending from the anterior perforated substance first laterally at the deep incisure between the frontal and temporal lobes, then back and slightly upward over the lateral aspect of the cerebral hemisphere, with the superior temporal gyrus as its lower bank, the insula forming its greatly expanded floor. Two short side branches, the ramus anterior and ramus ascendens, divide the inferior frontal gyrus into an orbital part, triangular part, and opercular part. Synonym: sulcus lateralis cerebri, fissura cerebri lateralis, lateral cerebral fissure, sylvian fissure, fissure of Sylvius. (05 Mar 2000) |
| layers of cerebral cortex | The outer portion of the brain, consisting of layersof nerve cells and the pathways that connect them. The cerebralcortex is the part of the brain in which thought processes take place.In Alzheimer's disease, nerve cells in the cerebral cortex die. (22 May 1997) |
| fusiform cells of cerebral cortex | Spindle-shaped cell's in the sixth layer of the cerebral cortex. (05 Mar 2000) |
| lunate cerebral sulcus | A small, inconstant semilunar groove on the cortical convexity near the occipital pole, marking the anterior border of the striate cortex (area 17) and considered homologous with the major sulcus of the same name that is a more constant feature of the cerebral cortex in monkeys and apes. Synonym: sulcus lunatus cerebri, ape fissure, lunate fissure, lunate sulcus, simian fissure. (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) |