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AVM arteriovenous malformation; atrioventricular malformation; aviation medicine
CM California mastitis [test]; calmodulin; capreomycin; carboxymethyl; cardiac murmur; cardiac muscle; ...
AVM Arterio-Venous Malformation
ACM acetaminophen; acute cerebrospinal meningitis; Adriamycin, cyclophosphamide, methotrexate; albumin- ...
AOIVM angiographically occult intracranial vascular malformation
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AOVM angiographically occult vascular malformation
ACM Arnold--Chiari malformation
CAVM cerebral arteriovenous malformation
CCM Cerebral cavernous malformation
C.C.A.M. Congenital Cystic Adenomatoid Malformation
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Mondini C., Italian physician, 1729-1803.
See: Mondini deafness, Mondini dysplasia.
(05 Mar 2000)
Mondini deafness The hearing loss resulting from the structural aberration of Mondini dysplasia.
(05 Mar 2000)
Mondini dysplasia Congenital anomaly of osseus and membranous labyrinth characterised by aplastic cochlea, and deformity of the vestibule and saemicircular canals with partial or complete loss of auditory and vestibular function; may be associated with spontaneous cerebrospinal fluid otorrhoea resulting in meningitis.
See: Mondini deafness.
(05 Mar 2000)
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)
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)
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