| DDS | damaged disc syndrome; dendrodendritic synaptosome; dental distress syndrome; depressed DNA synthesi... |
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| EDS | edema disease of swine; egg drop syndrome; Ehlers-Danlos syndrome; Emery-Dreifus syndrome; energy-di... |
| FS | factor of safety; Fanconi syndrome; Felty syndrome; fibromyalgia syndrome; field stimulation; Fisher... |
| GS | gallstone; Gardner syndrome; gastric shield; general surgery; gestational score; Gilbert syndrome; g... |
| HSS | Hallermann-Streiff syndrome; Hallervorden-Spatz syndrome; Henoch-Schonlein syndrome; high-speed supe... |
| facial surface of tooth | The surface of a tooth that faces the buccal or labial mucosa of vestibule of the mouth; opposite to the lingual surface of tooth. Synonym: facies vestibularis dentis, facies facialis dentis, buccal surface, facial surface of tooth, facies buccalis, facies labialis, labial surface. (05 Mar 2000) |
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| facial tic | Involuntary twitching of the facial muscles, sometimes unilateral. Synonym: Bell's spasm, convulsive tic, facial spasm, histrionic spasm, mimic convulsion, mimic spasm, mimic tic, palmus, prosopospasm. (05 Mar 2000) |
| facial tics | <neurology> A repetitive spasmodic movement of the eyes or facial muscles. May also involve the neck or shoulders. Tics are most common in children. The cause is unknown but may be linked to stress. Tics are more common in children with attention deficit hyperactivity disease. Most tics require no treatment and resolve on their own with patient education. (27 Sep 1997) |
| facial triangle | A triangle formed by lines connecting the basion, the prosthion, and the nasion. (05 Mar 2000) |
| facial trophoneurosis | Atrophy of one half of the face which is sometimes progressive, and is of unknown cause. (12 Dec 1998) |
| facial vein | <anatomy, vein> A continuation of the angular vein at the medial angle of the eye. It passes diagonally downward and outward, joining with the retromandibular vein below the border of the lower jaw before emptying into the internal jugular vein. Synonym: anterior facial vein, vena facialis anterior, vena facialis. (05 Mar 2000) |
| facial vision | <physiology> Sensing the proximity of objects by the nerves of the face, presumed in the case of the blind and also in sighted persons who are blindfolded or in darkness. (05 Mar 2000) |
| zygomatic branch of facial nerve | Branches of facial nerve crossing upper cheek to supply orbicularis oculi muscle. Synonym: rami zygomatici nervi facialis. (05 Mar 2000) |
| lateral crus of facial canal | Laterally-placed, posteriorly-directed second portion of the horizontal part of the facial canal. See: horizontal part of facial canal. Synonym: lateral crus of horizontal part of the facial canal. (05 Mar 2000) |
| lateral crus of horizontal part of the facial canal | Laterally-placed, posteriorly-directed second portion of the horizontal part of the facial canal. See: horizontal part of facial canal. Synonym: lateral crus of horizontal part of the facial canal. (05 Mar 2000) |
| lingual branch of facial nerve | Lingual branch (inconstant) of the stylohyoid branch of the facial nerve. Synonym: ramus lingularis nervi facialis. (05 Mar 2000) |
| lingual-facial-buccal dyskinesia | A syndrome of potentially irreversible, involuntary, dyskinetic movements that may develop in patients who have been treated with antipsychotic medications (for example phenothiazines) longer-term. Other drugs known to cause tardive dyskinesia include: tricyclic antidepressants, selegiline, clozapine, levamisole and metoclopramide. (27 Sep 1997) |
| 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) |