| LML | large and medium lymphocytes; left mediolateral; left middle lobe |
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| LUL | left upper eyelid; left upper limb; left upper lobe; left upper lung |
| ML | Licentiate in Medicine; Licentiate in Midwifery; malignant lymphoma; marked latency; maximum likelih... |
| NL | neural lobe; neutral lipid; nodular lymphoma; normal; normal libido, normal limits |
| PLB | parietal lobe battery; phospholamban; phospholipase B; porous layer bead |
| frontal sinus | One of the paired, but seldom symmetrical, air spaces located between the inner and outer compact layers of the frontal bone. (12 Dec 1998) |
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| frontal sinus aperture | One of a pair of openings in the floor of the frontal sinuses in the nasal part of the frontal bone, through which the frontal sinuses communicate with the ethmoidal infundibulum via the frontonasal duct. Synonym: apertura sinus frontalis. (05 Mar 2000) |
| frontal sinusitis | Inflammation of the frontal sinus; in most cases the infection is caused by the bacteria streptococcus pneumoniae and haemophilus influenzae. This condition may be acute or chronic. (12 Dec 1998) |
| frontal squama | The tabular or squamous portion of occipital bone. Synonym: squama occipitalis, occipital squama, frontal squama. (05 Mar 2000) |
| frontal suture | The suture between the two halves of the frontal bone, usually obliterated by about the sixth year; if persistent it is called a metropic suture. Synonym: sutura frontalis. (05 Mar 2000) |
| frontal triangle | A triangle bounded above by the maximum frontal diameter and laterally by lines joining the extremities of this diameter with the glabella. (05 Mar 2000) |
| frontal tuber | The most prominent portion of the frontal bone on either side. Synonym: tuber frontale, eminentia frontalis, frontal tuber. (05 Mar 2000) |
| frontal veins | The superficial veins draining the frontal cortex and emptying into the superior sagittal sinus. Synonym: supratrochlear veins. (05 Mar 2000) |
| frontal zone contraction theory | Model proposed to account for the movement of giant amoebae in which cytoplasmic contraction at the front of the leading pseudopod (fountain zone) pulls viscoelastic cytoplasm forward in the centre of the cell and forms a tube of more rigid cytoplasm immediately below the plasma membrane behind the active region. The peripheral contracted cytoplasm relaxes into a weaker gel at the rear and is pulled forward in its turn. Contrasts with the ectoplasmic tube contraction model. (18 Nov 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) |
| 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) |