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| ACM | acetaminophen; acute cerebrospinal meningitis; Adriamycin, cyclophosphamide, methotrexate; albumin- ... |
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| AVM | arteriovenous malformation; atrioventricular malformation; aviation medicine |
| CM | California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ... |
| BCS | battered child syndrome; blood cell separator; British Cardiac Society; Budd-Chiari syndrome |
| CF | calcaneal fibular [ligament]; calcium leucovorin; calf blood flow; calibration factor; cancer-free; ... |
| ACM | Arnold--Chiari malformation |
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| BCS | Budd Chiari syndrome |
| AOVM | angiographically occult vascular malformation |
| CAVM | cerebral arteriovenous malformation |
| CCM | Cerebral cavernous malformation |
| arnold-chiari malformation | <radiology> Chiari I herniation of medulla and cerebellar tonsils, 4th ventricle in normal position, Chiari II herniation of medulla, tonsils, vermis, 4th ventricle at foramen magnum, myelomeningocele, aqueductal stenosis most likely to be hydrocephalus, Chiari III further herniation, 4th ventricle below foramen magnum, encephalocele or myelomeningocele associated with: agenesis of corpus callosum, syrinx (12 Dec 1998) |
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| arteriovenous malformation | <anatomy, embryology> A tangled collection of abnormal blood vessels where there is an abnormal communication between the arterial and venous systems. The afferents flow directly into the venous efferents without the usual resistance of an intervening capillary bed. They are mostly congenital. If large enough, they may produce a shunt of sufficient magnitude to raise the cardiac output. Common sites include; skin, liver, brain, brainstem and spinal cord, where they may cause headaches, seizures or bleeding (subarachnoid haemorrhage). See: arteriovenous fistula, cerebral arteriovenous malformations. Synonym: haemangioma (20 Jun 2000) |
| A-V malformation | <anatomy, embryology> A tangled collection of abnormal blood vessels where there is an abnormal communication between the arterial and venous systems. The afferents flow directly into the venous efferents without the usual resistance of an intervening capillary bed. They are mostly congenital. If large enough, they may produce a shunt of sufficient magnitude to raise the cardiac output. Common sites include; skin, liver, brain, brainstem and spinal cord, where they may cause headaches, seizures or bleeding (subarachnoid haemorrhage). See: arteriovenous fistula, cerebral arteriovenous malformations. Synonym: haemangioma (20 Jun 2000) |
| malformation | <embryology> A morphologic defect resulting from an intrinsically abnormal developmental process. Origin: L. Malus = evil, formatio = a forming (18 Nov 1997) |
| cerebellomedullary malformation syndrome | <radiology> Chiari I herniation of medulla and cerebellar tonsils, 4th ventricle in normal position, Chiari II herniation of medulla, tonsils, vermis, 4th ventricle at foramen magnum, myelomeningocele, aqueductal stenosis most likely to be hydrocephalus, Chiari III further herniation, 4th ventricle below foramen magnum, encephalocele or myelomeningocele associated with: agenesis of corpus callosum, syrinx (12 Dec 1998) |
| congenital malformation | Abnormal formation of a structure evident at birth. (12 Dec 1998) |
| cystic adenomatoid malformation of lung | <radiology> Only true pulmonary cystic disease of newborn, three X-ray types: multicystic, walls of varying thickness, multicystic, one large dominant thin-walled cyst, solid, mediastinal shift common, cysts often contain foetal lung fluid, Treatment: surgery Cf: congenital lobar emphysema (12 Dec 1998) |
| cystic adenomatoid malformation of lung, congenital | A developmental anomaly that usually becomes apparent in the neonatal period with progressive respiratory distress. This malformation is a focal pulmonary dysplasia characterised by a multicystic mass of terminal bronchiolar structures. Ccam is classified into 3 separate types (I, II, III) depending on cyst size. (12 Dec 1998) |
| arnold-chiari deformity | A congenital anomaly in which the cerebellum and medulla oblongata, which is elongated and flattened, protrude down into the spinal canal through the foramen magnum. It may be associated with many other defects, including spina bifida occulta and meningomyelocele. (12 Dec 1998) |
| Arnold-Chiari syndrome | <radiology> Chiari I herniation of medulla and cerebellar tonsils, 4th ventricle in normal position, Chiari II herniation of medulla, tonsils, vermis, 4th ventricle at foramen magnum, myelomeningocele, aqueductal stenosis most likely to be hydrocephalus, Chiari III further herniation, 4th ventricle below foramen magnum, encephalocele or myelomeningocele associated with: agenesis of corpus callosum, syrinx (12 Dec 1998) |
| Budd-Chiari syndrome | <gastroenterology, syndrome> Liver dysfunction due to occlusion of the hepatic veins. May be congenital. (27 Sep 1997) |
| Chiari-Budd syndrome | <syndrome> Thrombosis of the hepatic vein with great enlargement of the liver and extensive development of collateral vessels, intractable ascites, and severe portal hypertension. Synonym: Budd's syndrome, Budd-Chiari syndrome, Chiari's disease, Chiari-Budd syndrome, Rokitansky's disease. (05 Mar 2000) |
| chiari-frommel syndrome | <syndrome> Persistent lactation and amenorrhoea following pregnancy. (12 Dec 1998) |
| Chiari, Hans | <person> German pathologist, 1851-1916. See: Arnold-Chiari deformity, Arnold-Chiari malformation, Arnold-Chiari syndrome, Chiari's disease, Chiari's net, Chiari's syndrome, Chiari II syndrome, Chiari-Budd syndrome, Budd-Chiari syndrome. (05 Mar 2000) |
| Chiari II syndrome | <syndrome> Elongation of medulla and cerebellar tonsils and vermis with displacement through the foramen magnum into the upper spinal canal; often associated with other cerebral anomalies. (05 Mar 2000) |
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