| 영문 | sensory nerve | 한글 | 감각신경 |
|---|---|---|---|
| 설명 | 감각세포가 받은 자극을 중추신경에 전달하는 신경. 눈이나 피부 등에 있는 감각기가 외부로부터 자극을 받으면 감각신경을 거쳐 척수와 대뇌겉질까지 감각이 전달된다. 이와 같이 외부로부터 내부를 향해 전달되는 감각신경은 구심성 신경계통이며, 원심성 운동신경계통 및 자율신경계통에 필적하는 말초신경의 하나이다. 이 감각신경에는 후각신경(뇌신경Ⅰ)-시각신경(뇌신경Ⅱ)-눈돌림신경(뇌신경Ⅲ)-삼차신경(뇌신경Ⅴ)-얼굴신경(뇌신경Ⅶ)-청각신경(뇌신경Ⅷ)-혀인두신경(뇌신경Ⅸ)-미주신경(뇌신경Ⅹ) 및 척수신경이 있다. 감각신경 중 미주신경을 제외하면 모두 두부에 분포되어 있고, 후각신경-시각신경-청각신경의 세가지는 특히 분화된 감각상피를 지배한다. 혀인두신경은 미각의 말단장치와 그 밖의 부분에 연결되고 미주신경은 흉강과 복강의 기관에 분포되어 구심성 충격을 중추에 전달하며 삼차신경은 척수의 각 마디에 있는 신경에 해당하여(머리의 피부-점막 등의 표면감각과 심부감각을 관장한다. 척수의 감각신경계통에도 피부와 심부, 내장의 분포에 따른 구별이 있다. |
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| 영문 | abnormality, anomaly | 한글 | 이상, 비정상 |
|---|---|---|---|
| 설명 | 정상을 벗어난 성질 혹은 사실. anomaly, aberration 등도 이상 상태를 나타내는 것이지만 abnormality가 가장 넓은 의미의 이상이다. anomaly는 보통 선천적 이상을 의미하며, aberration은 맨 눈으로 보이지 않는 이상을 의미하는 경우가 많다. |
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| HIVD | Herniation(Herniated) of Inter-Vertebral Disc - Cervical HIVD &... |
|---|---|
| JVP | [POMD P 49 - 52] 1) Jugular Vein Pressure 2) Jugular Venous Pulse ... |
| TOF | 1) Tetralogy Of Fallot ? CIx of Corrective Op ... |
| BCA | balloon catheter angioplasty; bicinchoninic acid; blood color analyzer; Blue Cross Association; bran... |
| CHIME | coloboma, heart anomaly, ichthyosis, mental retardation, ear abnormality |
| SAA | South Atlantic Anomaly |
|---|---|
| MCA | multiple congenital anomaly |
| HMSN | Hereditary Motor and Sensory Neuropathies |
| HMSN | Hereditary motor and sensory neuropathy |
| HMSN I | Hereditary motor and sensory neuropathy type 1 |
| Alder's anomaly | Coarse azurophilic granulation of leukocytes, especially granulocytes, which may be associated with gargoylism and Morquio's disease. (05 Mar 2000) |
|---|---|
| angle of anomaly | <ophthalmology> An obsolete term for the degree of deviation from parallelism of the visual axes of the eyes. (05 Mar 2000) |
| anomaly | A marked deviation from the normal standard, especially as a result of congenital defects. Origin: Gr. Anomalia (18 Nov 1997) |
| Aristotle's anomaly | When a small object is held between the first and second fingers crossed in such a way that it touches or presses upon skin surfaces which ordinarily are not pressed upon simultaneously by a single object, it is perceived falsely as two. (05 Mar 2000) |
| May-Hegglin anomaly | A disorder in which neutrophils and eosinophils contain basophilic structures known as Dohle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym: May-Hegglin anomaly. (05 Mar 2000) |
| pelger-huet anomaly | An inherited defect interfering with normal nuclear lobulation of neutrophils and eosinophils. The nuclei appear rodlike, spherical, or dumbbell-shaped and their structure is coarse and lumpy. (12 Dec 1998) |
| Pelger-Huet nuclear anomaly | Congenital inhibition of lobulation in the nuclei of neutrophilic leukocytes; most cells present band or bilobulate appearance, and only an occasional cell is trilobed; it is not associated with disease, but may be confused with leukocyte "shift to left"; autosomal dominant inheritance. (05 Mar 2000) |
| Chediak-Steinbrinck-Higashi anomaly | <syndrome> An autosomal recessive disorder characterised by the presence of giant lysosomal vesicles in phagocytes and in consequence poor bactericidal function due to deficient secretion of myeloperoxidase by lysosomes. There is some perturbation of microtubule dynamics. There are abnormalities of granulation and nuclear structure of all types of leukocytes with malformation of peroxidase-positive granules, cytoplasmic inclusions, and Dohle bodies, often with hepatosplenomegaly, lymphadenopathy, anaemia, thrombocytopenia, roentgenologic changes of bones, lungs and heart, skin and psychomotor abnormalities, and susceptibility to infection. The condition usually results in death in childhood, before the age of 10. Reported from humans, albino Hereford cattle, mink, beige mice and killer whale. Compare: chronic granulomatous disease. Inheritance: autosomal recessive. Synonym: Beguez Cesar disease, Chediak-Higashi disease, Chediak-Steinbrinck-Higashi anomaly. (21 May 1997) |
| Rieger's anomaly | Mesodermal dysgenesis of cornea and iris, producing pupillary anomalies, posterior embryotoxon, and secondary glaucoma. Synonym: Rieger's anomaly. (05 Mar 2000) |
| Peters' anomaly | <syndrome> A congenital disorder originating from faulty separation of embryonic structures; it results in bilateral central corneal opacities, with an anterior ring attachment of the iridic pupillary border and anterior polar cataracts; associated with short-limbed dwarfism; autosomal dominant inheritance. See: iridocorneal endothelial syndrome. Synonym: Peters' anomaly. (05 Mar 2000) |
| morning glory anomaly | <ophthalmology, syndrome> A congenital anomaly of the optic disk in which there is a funnel-shaped hypoplastic optic nerve, which has a dot of white tissue at the centre, surrounded by an elevated anulus of chorioretinal pigment. The retinal vessels seen are multiple narrow bands at the edge of the disk. (22 Sep 2002) |
| Hegglin's anomaly | A disorder in which neutrophils and eosinophils contain basophilic structures known as Dohle or Amato bodies and in which there is faulty maturation of platelets, with thrombocytopenia; autosomal dominant inheritance. Synonym: May-Hegglin anomaly. (05 Mar 2000) |
| Shone's anomaly | Coarctation of the aorta, subaortic stenosis, and stenosing ring of the left atrium found in association with a parachute mitral valve. (05 Mar 2000) |
| developmental anomaly | An anomaly established during intrauterine life; a congenital anomaly. (05 Mar 2000) |
| ebstein anomaly | <radiology> Tricuspid valve: abnormal formation and insertion, usually tricuspid insufficiency, right atrial enlargement (if severe, box-like heart), decreased pulmonary vascularity, cyanosis, severe at birth, mild in later childhood, angio: to-and-fro motion of contrast between RA and atrialised RV (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|