| ICE | ice, compression, elevation; ichthyosis-cheek-eyebrow [syndrome]; immunochemical evaluation; interle... |
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| ASMD | anterior segment mesenchymal dysgenesis; atonic sclerotic muscle dystrophy |
| ASOD | anterior segmental ocular dysgenesis |
| FDTS | familial testicular dysgenesis syndrome |
| GD | gastroduodenal; Gaucher disease; general diagnostics; general dispensary; gestational day; Gianotti ... |
| ICE | Iridocorneal endothelial |
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| MMMT | Malignant Mixed Mesodermal Tumor |
| MMT | Mixed mesodermal tumor |
| GD | Gonadal dysgenesis |
| MGD | Mixed gonadal dysgenesis |
| 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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| mesodermal | <biology> Pertaining to, or derived from, the mesoderm; as, mesodermal tissues. Source: Websters Dictionary (01 Mar 1998) |
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| mesodermal factor | A protein that can induce the formation of kidney and muscle primordia in embryos. (05 Mar 2000) |
| mixed mesodermal tumour | A sarcoma of the body of the uterus arising in older women, composed of more than one mesenchymal tissue, especially including striated muscle cells. Synonym: malignant mixed mullerian tumour. (05 Mar 2000) |
| mixed tumour, mesodermal | A sarcoma of the body of the uterus arising in older women, composed of more than one mesenchymal tissue, especially including striated muscle cells. It is associated with previous pelvic radiation exposure in 20% of patients. (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) |
| gonadal dysgenesis, mixed | A syndrome of gonadal dysgenesis in which there is a testis on one side and a "streak gonad" on the other. The phenotype is generally male, but may be female since the individual is a mosaic. Various karyotypes have been identified, including 45,xo/47,xyy; 45,xo/46,xy; and 45,xo/46,xyo. (12 Dec 1998) |
| seminiferous tubule dysgenesis | A disorder in which the seminiferous tubules exhibit an abnormal cytoarchitecture and extensive hyalinization; the testes are small, and few spermatozoa are formed; the body habitus may be eunuchoid, and gynaecomastia may be present; urinary gonadotropin output is usually high, and the incidence of mental deficiency and illness increased; sex chromatin may be male or female, and androgen secretion ranges from subnormal to normal. It is a constant feature of (and is often used synonymously with) Klinefelter's syndrome. Synonym: germinal aplasia. (05 Mar 2000) |
| hybrid dysgenesis | The inability of certain strains of the fruit fly Drosophila melanogaster to interbreed with each other because they produce offspring that are all sterile or offspring which have a high number of harmful mutations. (09 Oct 1997) |
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