| HCM | Hypertrophic Cardio-Myopathy = HCMP |
|---|---|
| LIMM | lethal infantile mitochondrial myopathy |
| MTM | Thayer-Martin, modified [agar]; myotubular myopathy |
| MTMX | myotubular myopathy, X-linked |
| XLMTM | X-linked myotubular myopathy |
| HOMO | Highest Occupied Molecular Orbital |
|---|---|
| LUMO | Lowest Unoccupied Molecular Orbital |
| MO | Molecular Orbital |
| VLO | ventrolateral orbital cortex |
| CNM | Centronuclear myopathy |
| carcinomatous myopathy | <syndrome> A condition characterised by muscle weakness that is similar to the symptoms of myasthenia gravis. For this reason, it has been referred to as myasthenic syndrome. This disorder is caused by an insufficient release of neurotransmitter (acetylcholine) by the nerve cells. Unlike myasthenia gravis, as muscle contractions are continued, strength will increase. The cause of Lambert-Eaton syndrome is unknown, but is usually associated with small cell carcinoma of the lung or an autoimmune illness. (27 Sep 1997) |
|---|---|
| centronuclear myopathy | Slowly progressive generalised muscle weakness and atrophy beginning in childhood; on biopsy of skeletal muscle, the nuclei of most muscle fibres are seen to be located near the centre of a small fibre (the normal position for a 10-week embryo) rather than at the periphery of the fibre; familial incidence. Autosomal dominant recessive and X-linked [310400] forms occur. Synonym: myotubular myopathy. Distal myopathy, myopathy affecting predominantly the distal portions of the limbs; onset is usually after age 40, with weakness and wasting of small muscles of the hands; The infantile form and the Swedish later-onset are autosomal dominant and there is a Japanese late-onset type that is recessive. Minicore-multicore myopathy, an uncommon nonprogressive myopathy with early onset, proximal weakness, and hypotonia. Muscle fibres show focal defects of oxidative and myofibrillar adenosine triphosphatase enzymes with disorganization of myofibril ultrastructure. Mitochondrial myopathy, weakness and hypotonia of muscles, primarily those of the neck, shoulder, and pelvic girdles, with onset in infancy or childhood; on biopsy, giant, bizarre mitochondria are seen located between muscle fibrils just beneath the sarcolemma. The dominant form is due to deletion of mitochondrial DNA and the recessive form is due to a complex deficiency. (05 Mar 2000) |
| rod myopathy | A congenital myofibrillar abnormality in which small threadlike or rod-shaped bodies are scattered through the muscle fibres. It is marked by hypotonia and proximal muscle weakness. It is also called rod myopathy with reference to the threadlike (greek nema, thread) rods or myofibrils (latin fibrilla, a little fibre or threadlike structure). (12 Dec 1998) |
| myopathy | <neurology> Any disease of a muscle. Origin: Gr. Pathos = disease (18 Nov 1997) |
| myotubular myopathy | Slowly progressive generalised muscle weakness and atrophy beginning in childhood; on biopsy of skeletal muscle, the nuclei of most muscle fibres are seen to be located near the centre of a small fibre (the normal position for a 10-week embryo) rather than at the periphery of the fibre; familial incidence. Autosomal dominant recessive and X-linked [310400] forms occur. Synonym: myotubular myopathy. Distal myopathy, myopathy affecting predominantly the distal portions of the limbs; onset is usually after age 40, with weakness and wasting of small muscles of the hands; The infantile form and the Swedish later-onset are autosomal dominant and there is a Japanese late-onset type that is recessive. Minicore-multicore myopathy, an uncommon nonprogressive myopathy with early onset, proximal weakness, and hypotonia. Muscle fibres show focal defects of oxidative and myofibrillar adenosine triphosphatase enzymes with disorganization of myofibril ultrastructure. Mitochondrial myopathy, weakness and hypotonia of muscles, primarily those of the neck, shoulder, and pelvic girdles, with onset in infancy or childhood; on biopsy, giant, bizarre mitochondria are seen located between muscle fibrils just beneath the sarcolemma. The dominant form is due to deletion of mitochondrial DNA and the recessive form is due to a complex deficiency. (05 Mar 2000) |
| nemaline myopathy | A congenital myofibrillar abnormality in which small threadlike or rod-shaped bodies are scattered through the muscle fibres. It is marked by hypotonia and proximal muscle weakness. It is also called rod myopathy with reference to the threadlike (greek nema, thread) rods or myofibrils (latin fibrilla, a little fibre or threadlike structure). (12 Dec 1998) |
| ocular myopathy | A specific type of slowly worsening weakness of the ocular muscles, usually associated with a pigmentary retinopathy. See: Kearns-Sayre syndrome, oculopharyngeal dystrophy. Synonym: ocular myopathy. (05 Mar 2000) |
| thyrotoxic myopathy | Extreme muscular weakness in severe thyrotoxicosis affecting muscles of limbs and trunk as well as those used in speech and swallowing. (05 Mar 2000) |
| bilateral medial orbital ecchymoses | <clinical sign, ophthalmology> The appearance of the eyes produced by subconjunctival haemorrhage and/or periorbital ecchymosis. Synonym: bilateral medial orbital ecchymoses. (21 Jun 2000) |
| cephalo-orbital index | The ratio of the cubic content of the two orbits to that of the cranial cavity multiplied by 100. (05 Mar 2000) |
| granuloma, plasma cell, orbital | A distinctive, chronic inflammatory reaction in the orbital tissues of the eye, of unknown aetiology, that may closely resemble a neoplasm and often becomes bilateral. Symptoms include exophthalmos and congestion of the lids with oedema. When limitation of ocular motility also occurs, it is sometimes called orbital myositis. (12 Dec 1998) |
| spheno-orbital suture | Articulation between the orbital process of the palatine bone and the outer surface of the body of the sphenoid. Synonym: sutura spheno-orbitalis. (05 Mar 2000) |
| superior orbital fissure | A cleft between the greater and the lesser wings of the sphenoid establishing a channel of communication between the middle cranial fossa and the orbit, through which pass the oculomotor and trochlear nerves, the ophthalmic division of the trigeminal nerve, the abducens nerve, and the ophthalmic veins. Synonym: fissura orbitalis superior, foramen lacerum anterius, sphenoidal fissure. (05 Mar 2000) |
| inferior orbital fissure | A cleft between the greater wing of the sphenoid and the orbital plate of the maxilla, through which pass the maxillary division and the orbital branch of the trigeminal nerve, fibres from the pterygopalatine (Meckel's) ganglion, and the infraorbital vessels. Synonym: fissura orbitalis inferior, sphenomaxillary fissure. (05 Mar 2000) |
| orbital | <anatomy> Pertaining to the orbit, which is the bony cavity containing the eyeball. (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|