| MBH | medial basal hypothalamus |
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| ME-BH | medial eminence of basal hypothalamus |
| BM | Bachelor of Medicine; barium meal; basal medium; basal metabolism; basement membrane; basilar membra... |
| ABA | abscissic acid; allergic bronchopulmonary aspergillosis; American Board of Anesthesiologists; antiba... |
| ABPA | actin-binding protein, autosomal form; allergic bronchopulmonary aspergillosis |
| bronchopulmonary sequestration | A developmental anomaly in which a mass of nonfunctioning lung tissue lacks normal connection with the tracheobroncheal tree and receives an anomalous blood supply originating from the descending thoracic or abdominal aorta. The mass may be extralobar, i.e., completely separated from normally connected lung, or intralobar, i.e., partly surrounded by normal lung. (12 Dec 1998) |
|---|---|
| bronchopulmonary spirochetosis | Chronic bronchitis due to infection with spirochetes (though other bacteria are usually present and contribute to the infection) and characterised by cough and bloody sputum. Synonym: bronchopulmonary spirochetosis, bronchospirochetosis, Castellani's bronchitis. (05 Mar 2000) |
| glycogen storage disease type VII | <disease> An autosomal recessive muscle glycogen storage disease in which there is deficient expression of muscle phosphofructokinase activity, resulting in increased concentrations of glucose-6-phosphate and fructose-6-phosphate and low concentrations of fructose-1,6-diphosphate in muscle tissue. Glycogen storage in muscle is increased, perhaps due to activation of glycogen synthase by accumulated glucose-6-phosphate. It has been proposed that shunting of glucose-6-phosphate and fructose-6-phosphate into the pentose phosphate pathway may result in increased synthesis of purines and pyrimidines, causing hyperuricaemia and gout. Erythrocytes from patients may show decreased phosphofructokinase activity and 2,3-diphosphoglycerate deficiency. Exercise intolerance is present and severe congenital muscular dystrophy has been reported. Inheritance: autosomal recessive (12 Dec 1998) |
| mucopolysaccharidosis vii | Mucopolysaccharidosis characterised by excessive dermatan and heparan sulfates in the urine and hurler-like features. It is caused by a deficiency of beta-glucuronidase. (12 Dec 1998) |
| cranial mononeuropathy vii | A disorder which involves drooping of the face and the decreased ability to move one side of the face. Causes include isolated damage to the facial nerve, HIV infection, sarcoidosis and Lyme disease. Bell's palsy is a dysfunction of the facial nerve for reason unknown. (27 Sep 1997) |
| cranial nerve VII | <anatomy, nerve> The facial nerve enervates the muscles of the face (facial expression). Lesion of the facial nerve cause a drooping to one side of the face, inability to wrinkle the forehead, inability to whistle, inability to close the eye and deviation of the mouth to the unaffected side. Synonym: cranial nerve VII. (27 Sep 1997) |
| type VII mucopolysaccharidosis | <syndrome> An autosomal recessive disorder due to a deficiency of a beta-glucuronidase; defective lysosomal degradation of dermatan sulfate, heparan sulfate, and chondroitin sulfate; cellular function disrupted in most tissues. Synonym: type VII mucopolysaccharidosis, type VIII mucopolysaccharidosis. (05 Mar 2000) |
| exonuclease vii | An exonuclease enzyme which makes oligonucleotides by cleaving chunks of nucleotides off of both ends of single-stranded DNA. (09 Oct 1997) |
| factor vii | <chemical> Heat- and storage-stable plasma protein that is activated by tissue thromboplastin to form factor viia in the extrinsic pathway of blood coagulation. The activated form then catalyses the activation of factor x to factor xa. Chemical name: Blood-coagulation factor VII (12 Dec 1998) |
| factor vii assay | A test used to measure the activity of a blood clotting factor VII. This test may be used to evaluate excessive bleeding. Abnormally low factor VII assays may be seen in the following conditions: congenital deficiency of factor VII, fat malabsorption, heparin administration, cirrhosis, vitamin K deficiency and warfarin administration. (27 Sep 1997) |
| factor vii deficiency | An inherited disorder that causes abnormal blood clotting due to the congenital absence of one of the 20 different plasma proteins involved in the coagulation process. Symptoms include bleeding of the gums, nosebleeds, easy bruising, bleeding in muscles or joints and excessive menstrual bleeding. Treatment includes the administration of plasma concentrates of factor VII (extrinsic factor). (27 Sep 1997) |
| anterior eye segment | That part of the eyeball anterior to the lens. (12 Dec 1998) |
| anterior inferior segment | Anterior inferior segment of kidney. Synonym: segmentum anterius inferius. (05 Mar 2000) |
| anterior ocular segment | That portion of the eye comprising the cornea, iris, lens, and their associated chambers and adnexa. (05 Mar 2000) |
| anterior segment | A delimited part or section of an organ or other structure which lies in front of or ventral to the other similar parts or sections. 1) segmentum anterius (hepar); the anterior segment of the right lobe of the liver. 2) segmentum anterius (pulmo dexter et sinister); [S 3]; the anterior segment of the superior lobe of the right and left lungs. 3) anterior segment of the eye; the intraocular segment of the eyeball occupied by the aqueous which lies in front of, and is separated from the vitreous-filled posterior segment by, the lens and zonule; it is subdivided by the iris into anterior and posterior chambers. Synonym: segmentum anterius. (05 Mar 2000) |