Medical Conditions Dictionary http://medconditions.net Dictionary of over 120,000 medical conditions terminology defined and explained in easy yet professional tone. Wed, 26 Jun 2013 20:46:34 +0000 en hourly 1 http://wordpress.org/?v=3.2.1 Muscular, Peroneal Atrophy http://medconditions.net/muscular-peroneal-atrophy.html http://medconditions.net/muscular-peroneal-atrophy.html#comments Wed, 26 Jun 2013 20:46:34 +0000 Admin http://medconditions.net/muscular-peroneal-atrophy.html A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)

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Muscular, Spinobulbar Atrophy http://medconditions.net/muscular-spinobulbar-atrophy.html http://medconditions.net/muscular-spinobulbar-atrophy.html#comments Wed, 26 Jun 2013 08:46:37 +0000 Admin http://medconditions.net/muscular-spinobulbar-atrophy.html Disorders characterized by an abnormal reduction in muscle volume due to a decrease in the size or number of muscle fibers. Atrophy may result from diseases intrinsic to muscle tissue (e.g., MUSCULAR DYSTROPHY) or secondary to PERIPHERAL NERVOUS SYSTEM DISEASES that impair innervation to muscle tissue (e.g., MUSCULAR ATROPHY, SPINAL).

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Mycotic Aneurysm http://medconditions.net/mycotic-aneurysm.html http://medconditions.net/mycotic-aneurysm.html#comments Tue, 25 Jun 2013 20:46:28 +0000 Admin http://medconditions.net/mycotic-aneurysm.html Aneurysm due to growth of microorganisms in the arterial wall, or infection arising within preexisting arteriosclerotic aneurysms.

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Myelomonocytic Differentiation Antigens http://medconditions.net/myelomonocytic-differentiation-antigens.html http://medconditions.net/myelomonocytic-differentiation-antigens.html#comments Tue, 25 Jun 2013 08:46:23 +0000 Admin http://medconditions.net/myelomonocytic-differentiation-antigens.html Surface antigens expressed on myeloid cells of the granulocyte-monocyte-histiocyte series during differentiation. Analysis of their reactivity in normal and malignant myelomonocytic cells is useful in identifying and classifying human leukemias and lymphomas.

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Myelopathic Muscular Atrophy http://medconditions.net/myelopathic-muscular-atrophy.html http://medconditions.net/myelopathic-muscular-atrophy.html#comments Mon, 24 Jun 2013 20:46:19 +0000 Admin http://medconditions.net/myelopathic-muscular-atrophy.html A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)

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Myelophthisic Anemia http://medconditions.net/myelophthisic-anemia.html http://medconditions.net/myelophthisic-anemia.html#comments Mon, 24 Jun 2013 08:46:36 +0000 Admin http://medconditions.net/myelophthisic-anemia.html Anemia characterized by appearance of immature myeloid and nucleated erythrocytes in the peripheral blood, resulting from infiltration of the bone marrow by foreign or abnormal tissue.

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Myoclonic Astatic Epilepsy http://medconditions.net/myoclonic-astatic-epilepsy.html http://medconditions.net/myoclonic-astatic-epilepsy.html#comments Sun, 23 Jun 2013 20:46:29 +0000 Admin http://medconditions.net/myoclonic-astatic-epilepsy.html A clinically diverse group of epilepsy syndromes characterized either by myoclonic seizures or by myoclonus in association with other seizure types. Myoclonic epilepsy syndromes are divided into three subtypes based on etiology: familial, cryptogenic, and symptomatic (i.e., occurring secondary to known disease processes such as infections, hypoxic-ischemic injuries, trauma, etc.).

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Myosin ATPase http://medconditions.net/myosin-atpase.html http://medconditions.net/myosin-atpase.html#comments Sun, 23 Jun 2013 08:46:20 +0000 Admin http://medconditions.net/myosin-atpase.html A diverse superfamily of proteins that function as translocating proteins. They share the common characteristics of being able to bind ACTINS and hydrolyse MgATP. Myosins generally consist of heavy chains which are involved in locomotion, and light chains which are are involve in regulation. Within the structure of myosin heavy chain are three domains: the head, the neck and the tail. The head region of the heavy chain contains the actin binding domain and MgATPase domain which provides energy for locomotion. The neck region is involved in binding the light-chains. The tail region provides the anchoring point that maintains the position of the heavy chain. The superfamily of myosins is organized into structural classes based upon the type and arrangement of the subunits they contain.

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Narcotic Antagonists http://medconditions.net/narcotic-antagonists.html http://medconditions.net/narcotic-antagonists.html#comments Sat, 22 Jun 2013 20:46:44 +0000 Admin http://medconditions.net/narcotic-antagonists.html Agents inhibiting the effect of narcotics on the central nervous system.

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NASBA Analysis http://medconditions.net/nasba-analysis.html http://medconditions.net/nasba-analysis.html#comments Sat, 22 Jun 2013 08:46:42 +0000 Admin http://medconditions.net/nasba-analysis.html An isothermal in-vitro nucleotide amplification process. The process involves the concomitant action of a RNA-DIRECTED DNA POLYMERASE, a ribonuclease (RIBONUCLEASES), and a DNA-DIRECTED RNA POLYMERASE to synthesize large quantities of sequence-specific RNA and DNA molecules.

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