| RUX | right upper extremity |
|---|---|
| u/ext | upper extremity |
| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| CHA | Canadian Hospital Association; Catholic Health Association; Chinese hamster; chronic hemolytic anemi... |
| upper lip | The muscular fold forming the superior border of the mouth. Synonym: labium superius oris. (05 Mar 2000) |
|---|---|
| upper lobe of lung | The lobe of the right lung that lies above the oblique and horizontal fissures and includes the apical, posterior and anterior bronchopulmonary segments; in the left lung, the lobe lies above the oblique fissure and contains the apicoposterior, anterior, superior lingular and inferior lingular segments. Synonym: lobus superior pulmonis, upper lobe of lung. (05 Mar 2000) |
| upper/lower lobe predominance | <radiology> Upper lobe, usually site of greatest disease due to poorer clearance, bronchogenic carcinoma, pneumoconioses, histiocytosis X, sarcoidosis, ankylosing spondylitis, lower lobe, scleroderma (12 Dec 1998) |
| upper motor neuron | Clinical term indicating those neuron's of the motor cortex that contribute to the formation of the pyramidal or corticospinal and corticobulbar tracts, as distinguished from the lower motor neuron's innervating the skeletal muscles. Although not motor neuron's in the strict sense, these cortical neuron's became colloquially classified as motor neuron's because their stimulation produces movement and their destruction causes severe disorders of movement. See: motor neuron, motor cortex. (05 Mar 2000) |
| upper motor neuron lesion | Injury to cerebral descending (corticonuclear) fibres above the brainstem or spinal motor nerve nucleus. Synonym: upper motor neuron lesion. (05 Mar 2000) |
| upper nodal extrasystole | An obsolete term for a nodal extrasystole supposed to arise from the upper part of the A-V node; recognised in the electrocardiogram by a retrograde P wave preceding the QRS complex by an abnormally short P-R interval. (05 Mar 2000) |
| upper respiratory infection | Any number of viral or bacterial infections that includes infections of the throat, nasopharynx, sinuses, larynx, trachea or bronchi. (27 Sep 1997) |
| upper respiratory tract | The nasopharynx, oral cavity, and throat. (09 Oct 1997) |
| upper subscapular nerve | Two branches of the posterior cord of the brachial plexus, an upper and lower, supplying the subscapularis muscle; the lower subscapular nerve also supplies the teres major muscle. Synonym: nervi subscapulares. (05 Mar 2000) |
| upper thoracic splanchnic nerves | Part of the cardiopulmonary splanchnic nerves from the second to fifth segments of the thoracic sympathetic trunk that pass medially and anteriorly to enter the cardiac plexus; they convey postsynaptic sympathetic fibres to, and visceral afferent (pain) fibres from, the heart. Synonym: nervi cardiaci thoracici, upper thoracic splanchnic nerves. (05 Mar 2000) |
| upper uterine segment | The main portion of the body of the gravid uterus, the contraction of which furnishes the chief force of expulsion in labour. (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |