| ASMD | anterior segment mesenchymal dysgenesis; atonic sclerotic muscle dystrophy |
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| ICE | ice, compression, elevation; ichthyosis-cheek-eyebrow [syndrome]; immunochemical evaluation; interle... |
| BMT | Bachelor of Medical Technology; basement membrane thickening; benign mesenchymal tumor; bone marrow ... |
| HEPM | human embryonic palatal mesenchymal [cell] |
| ASOD | anterior segmental ocular dysgenesis |
| ICE | Iridocorneal endothelial |
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| EMT | Epithelial-mesenchymal transformation |
| EMT | Epithelial-mesenchymal transition |
| GD | Gonadal dysgenesis |
| MSC | Mesenchymal stem cells |
| iridocorneal mesodermal dysgenesis | Mesodermal dysgenesis of cornea and iris, producing pupillary anomalies, posterior embryotoxon, and secondary glaucoma. Synonym: Rieger's anomaly. (05 Mar 2000) |
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| mesenchymal | Relating to the mesenchyme. (05 Mar 2000) |
| mesenchymal cells | Fusiform or stellate cell's found between the ectoderm and endoderm of young embryos; the shape of the cell's in fixed material is indicative of the fact that in life they were moving from their place of origin to areas where they would become reaggregated and specialised; most mesenchymal cell's are derived from established mesodermal layers, but in the cephalic region they also develop from neural crest or neural tube ectoderm; they are the most strikingly pluripotential cell's in the embryonic body, developing at different locations into any of the types of connective or supporting tissues, to smooth muscle, to vascular endothelium, and to blood cells. (05 Mar 2000) |
| mesenchymal epithelium | The flat epithelium derived from mesenchymal cells found lining certain connective tissue spaces such as the anterior chamber of eye, perilymph spaces in the ear, and subdural and subarachnoid spaces. (05 Mar 2000) |
| mesenchymal hyloma | <tumour> A neoplasm of tissue derived from the mesoblastic pulp or mesenchyme. (05 Mar 2000) |
| mesenchymal tissue | Embryonic connective tissue. See: mesenchyme. (05 Mar 2000) |
| chondrosarcoma, mesenchymal | A rare aggressive variant of chondrosarcoma, characterised by a biphasic histologic pattern of small compact cells intermixed with islands of cartilaginous matrix. Mesenchymal chondrosarcomas have a predilection for flat bones; long tubular bones are rarely affected. They tend to occur in the younger age group and are highly metastatic. (devita jr et al., cancer: principles & practice of oncology, 3d ed, p1456) (12 Dec 1998) |
| pectinate ligaments of iridocorneal angle | The network of fibres (pectinate ligaments) at the iridocorneal angle between the anterior chamber of the eye and the venous sinus of the sclera; it contains spaces between the fibres that are involved in drainage of the aqueous humor, and is composed of two portions: the corneoscleral part, the part attached to the sclera, and the uveal part, the part attached to the iris. Synonym: reticulum trabeculare sclerae, Gerlach's valvula, Hueck's ligament, ligamentum annulare bulbi, pectinate ligaments of iridocorneal angle, pillar of iris, trabecular meshwork, trabecular network, trabecular zone. (05 Mar 2000) |
| spaces of iridocorneal angle | Irregularly shaped endothelium-lined spaces within the trabecular reticulum, through which the aqueous filters to reach the sinus venosus sclerae. Synonym: spatia anguli iridocornealis, ciliary canals, Fontana's spaces. (05 Mar 2000) |
| iridocorneal | Relating to the iris and the cornea. (05 Mar 2000) |
| iridocorneal angle | The acute angle between the iris and the cornea at the periphery of the anterior chamber of the eye. Synonym: angulus iridocornealis, angle of iris, angulus iridis, filtration angle. (05 Mar 2000) |
| iridocorneal endothelial syndrome | <syndrome> Syndrome of glaucoma, iris atrophy, decreased corneal endothelium, anterior peripheral synechia, and multiple iris nodules. Synonym: Cogan-Reese syndrome, iris-nevus syndrome. (05 Mar 2000) |
| iridocorneal syndrome | <syndrome> Iris atrophy with corneal oedema. Synonym: iridocorneal syndrome. (05 Mar 2000) |
| gonadal dysgenesis | <embryology, genetics> A rare genetic disorder in women that is characterised by the absence of an X chromosome. This disorder inhibits normal sexual development and causes infertility. Features include webbing of the neck, short stature, retarded development of secondary sex characteristics, absence of menses, coarctation of the aorta, low hairline, eye abnormalities (drooping eyelids) and skeletal deformities. Treatment include oestrogen supplementation at puberty. Growth hormone replacement may be necessary in some cases. Cardiac surgery may be necessary to correct coarctation of the aorta. Incidence: 1 in 3,000 births. (10 Oct 1997) |
| gonadal dysgenesis, 46,xy | A syndrome characterised by "streak gonads" in a phenotypic female with a 46,xy karyotype. It is due to a mutation which inhibits the function of the y-borne determinant that would normally cause the indifferent embryonic gonad to differentiate into a testis. The streak gonad is incapable of ovulation or oestrogen secretion. The syndrome is sometimes called "pure gonadal dysgenesis," but this designation may also refer to the presence of streak gonads with a 46,xx karyotype. (12 Dec 1998) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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