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  • steatocystoma multiplex
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AMC academic medical center; acetylmethyl carbinol; Animal Medical Center; antibody-mediated cytotoxicit...
XTM xanthoma tuberosum multiplex
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AMC Arthrogryposis Multiplex Congenita
M-FISH Multiplex-fluorescence in situ hybridization
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    Mononeuritis multiplex
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mononeuritis multiplex <endocrinology, neurology> A condition characterised by inflammation of several nerves in unrelated portions of the body, may be seen in association with long-standing diabetes.
(27 Sep 1997)
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mononeuritis Inflammation of a single nerve.
(05 Mar 2000)
arthrogryposis multiplex congenita Limitation of range of joint motion and contractures present at birth, usually involving multiple joints; a syndrome probably of diverse aetiology that may result from changes in spinal cord, muscle, or connective tissue. Several forms exist, autosomal dominant, recessive, and X-linked.
Synonym: amyoplasia congenita.
(05 Mar 2000)
paramyoclonus multiplex Synonym: myoclonus multiplex.
Origin: para-+ G. Mys, muscle, + klonos, a tumult
(05 Mar 2000)
myoclonus multiplex An ill-defined disorder marked by rapid and widespread muscle contractions.
Synonym: paramyoclonus multiplex, polyclonia, polymyoclonus.
(05 Mar 2000)
haemangioendothelioma tuberosum multiplex An eruption of pinkish papules, caused by hyperplasia of the endothelium of the superficial blood vessels.
(05 Mar 2000)
xanthoma multiplex <dermatology, pathology> An accumulation of an excess of lipids in the body due to disturbance of lipid metabolism and marked by the formation of foam cells in skin lesions.
(16 Dec 1997)
steatocystoma multiplex Widespread, multiple, thin-walled cysts of the skin that are lined by squamous epithelium, including lobules of sebaceous cells.
(05 Mar 2000)
dysostosis multiplex <syndrome> Mucopolysaccharidosis in which there is a deficiency of alpha-l-iduronidase, an accumulation of an abnormal intracellular material, and excretion of dermatan sulfate and heparan sulfate in the urine; with severe abnormality in development of skeletal cartilage and bone, with dwarfism, kyphosis, deformed limbs, limitation of joint motion, spadelike hand, corneal clouding, hepatosplenomegaly, mental retardation, and gargoyle-like facies; autosomal recessive inheritance.
See: mucolipidosis.
Synonym: dysostosis multiplex, Hurler's disease, lipochondrodystrophy, Pfaundler-Hurler syndrome, type IH mucopolysaccharidosis.
(05 Mar 2000)
dysplasia epiphysialis multiplex A dominantly inherited abnormality of epiphyses characterised by difficulty in walking, pain and stiffness of joints, stubby fingers, and often dwarfism of short-limb type; on X-ray examination, the epiphyses are mottled and irregular; ossification centres are late in appearance and may be multiple, but the vertebrae are normal. There is also an autosomal recessive form .
Synonym: dysplasia epiphysialis multiplex.
(05 Mar 2000)
lymphangioma tuberosum multiplex A cutaneous lesion characterised by multiple, slightly red, cystlike nodules (located chiefly on the trunk), resulting from fairly large lymphatic vessels and spaces, and groups of proliferating endothelial cells; the lesion has some gross resemblance to spiradenoma, except for the characteristic location.
(05 Mar 2000)
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mononeuritis multiplex A rare type of neuropathy that has been described with HIV infection. It may fall into two different categories. One type occurs during the early period of the infection and has a more benign outcome. The second form occurs later and is more aggressive, leading to progressive paralysis and death in some patients. It has been suggested that MM is related to multifocal cytomegalovirus (CMV) infection.
Ãâó: www.amfar.org/cgi-bin/iowa/bridge.html
mononeuritis multiplex a rare type of NEUROPATHY that causes patchy areas of movement and asymmetrical sensory abnormalities. MM tends to occur during the ASYMPTOMATIC, early period of HIV infection, but a more severe type, attributed to CYTOMEGALOVIRUS (CMV) infection, has been observed in people with advanced AIDS.
Ãâó: www.gmhc.org/health/glossary3.html
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