| DTR | Deep Tendon Reflex *** Deep Tendon Reflex(DTR)ÀÇ Center *** 1. ÇÏ¾Ç ¹Ý»ç; ... |
|---|---|
| ECG | Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ = EKG 1. Conducting System Structu... |
| DS | dead air space; dead space; deep sedative; deep sleep; defined substrate; dehydroepiandrosterone sul... |
| HCM | Hypertrophic Cardio-Myopathy = HCMP |
| LIMM | lethal infantile mitochondrial myopathy |
| CNM | Centronuclear myopathy |
|---|---|
| MM | Miyoshi myopathy |
| MTM1 | Myotubular myopathy |
| PROMM | Proximal myotonic myopathy |
| IIM | idiopathic inflammatory 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) |
| medial pectoral nerve | <anatomy, nerve> A nerve that arises from the medial cord of the brachial plexus to supply the pectoral muscles; usually pierces pectoralis minor, then continues to supply mainly the sternocostal portion of pectoralis major. Synonym: nervus pectoralis medialis, medial anterior thoracic nerve. (05 Mar 2000) |
| pectoral | 1. Of or pertaining to the breast, or chest; as, the pectoral muscles. 2. Relating to, or good for, diseases of the chest or lungs; as, a pectoral remedy. 3. <zoology> Having the breast conspicuously coloured; as, the pectoral sandpiper. <anatomy> Pectoral arch, or Pectoral girdle, the jacksnipe . Origin: L. Pectoralis, fr. Pectus, -oris the breast; cf. F. Pectoral. 1. A covering or protecting for the breast. 2. A breastplate, especially. That worn by the Jewish high person. A clasp or a cross worn on the breast. 3. A medicine for diseases of the chest organs, especially the lungs. Origin: L. Pectorale a breastplate, neut. Of pectorials. Source: Websters Dictionary (01 Mar 1998) |
| pectoral and abdominal anterior cutaneous branch of intercostal nerves | The ventral primary rami of spinal nerves T7-T11 (seventh to eleventh intercostal nerves), which supply the abdominal as well as the thoracic wall; innervate intercostal, subcostal, serratus posterior inferior, transversus abdominis, external and internal oblique, and rectus abdominis muscles, and provide sensory branches to the periphery of the diaphragm, and parietal pleura and peritoneum. Synonym: rami cutanei anteriores pectoralis et abdominalis nervorum intercostalium, ramus cutaneus anterior (pectoralis et abdominalis) nervorum thoracicorum, anterior cutaneous nerves of abdomen, pectoral and abdominal anterior cutaneous branch of intercostal nerves. (05 Mar 2000) |
| pectoral branch of thoracoacromial artery | <anatomy, artery> Branches of the thoracoacromial artery descending between and supplying the pectoralis major and minor muscles, then continuing to supply the serratus anterior muscle and, in the adult female, the upper portion of the breast. Synonym: rami pectorales arteriae thoracoacromialis. (05 Mar 2000) |
| pectoral fascia | The fascia that covers the pectoralis major muscle; it is attached to the sternum and to the clavicle; laterally and below it is continuous with the fascia of the shoulder, axilla, and thorax. Synonym: fascia pectoralis. (05 Mar 2000) |
| pectoral girdle | shoulder girdle |
| pectoral glands | Numerous nodes around the axillary veins which receive the lymphatic drainage from the upper limb, scapular region and pectoral region (including mammary gland); they drain into the subclavian trunk. Synonym: nodi lymphatici axillares, axillary glands. (05 Mar 2000) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|