| PDR | pediatric radiology; peripheral diabetic retinopathy; Physicians' Desk Reference; postdelivery room;... |
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| CDP | chondrodysplasia punctata; chronic destructive periodontitis; collagenase-digestible protein; contin... |
| CDPR | chondrodysplasia punctata, rhizomelic |
| CDPX | X-linked chondrodysplasia punctata |
| CP | candle power; capillary pressure; cardiac pacing; cardiac performance; cardiopulmonary; caudate puta... |
| RCDP | Rhizomelic Chondrodysplasia Punctata |
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| CAR | Cancer-associated retinopathy |
| C.S.R. | Central Serous Retinopathy |
| CRYO-ROP | Cryotherapy for Retinopathy of Prematurity |
| DRS | Diabetic Retinopathy Study |
retoperithelium
| retinopathy punctata albescens | A disease in which both fundi show numerous white dots through the retina; causes night blindness. (05 Mar 2000) |
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| acne punctata | Acne with black open comedones. (05 Mar 2000) |
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| chondrodysplasia punctata | A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (chondrodysplasia punctata, rhizomelic), an autosomal dominant form (conradi-hunermann syndrome), and a milder x-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form. (12 Dec 1998) |
| chondrodysplasia punctata, rhizomelic | An autosomal recessive form of chondrodysplasia punctata characterised by defective plasmalogen biosynthesis and impaired peroxisomes. Patients have shortened proximal limbs and severely disturbed endochondrial bone formation. The metabolic defects associated with the impaired peroxisomes are present only in the rhizomelic form of chondrodysplasia punctata. (12 Dec 1998) |
| chondrodystrophia congenita punctata | Congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma; there is also an autosomal dominant inheritance pattern . Synonym: chondrodystrophia congenita punctata. (05 Mar 2000) |
| Cooperia punctata | Species that occurs mainly in cattle, less commonly in sheep, water buffalo, and several wild ruminants; although worldwide in distribution, it is especially widespread in North America and common in Hawaii. Synonym: Cooperia fieldingi. (05 Mar 2000) |
| Haemaphysalis cinnabarina punctata | A race of Haemaphysalis in Europe, north Africa, and Japan; larvae and nymphs feed on terrestrial reptiles, and adults on various domestic herbivores, rabbits, and hedgehogs; it transmits bovine babesiosis and anaplasmosis. (05 Mar 2000) |
| psoriasis punctata | Psoriasis in which the individual lesions are papules, each red in colour, and tipped with a single white scale. (05 Mar 2000) |
| dysplasia epiphysialis punctata | A developmental error of the epiphyses characterised by severe deformities, epiphyses ossified from several discrete centres and with a stippled appearance, and thickened shafts of the long bones; congenital cataract and mental retardation are often present. There is an autosomal dominant form and an autosomal recessive form. Synonym: chondrodysplasia punctata, chondrodystrophia calcificans congenita, hypoplastic foetal chondrodystrophy, stippled epiphysis. (05 Mar 2000) |
| keratosis punctata | Horny papules over the palms, soles, and digits that develop central plugs; seen commonly in blacks. Synonym: keratoma disseminatum, keratosis punctata. (05 Mar 2000) |
| arteriosclerotic retinopathy | Retinopathy distinguished by attenuated retinal arterioles with increased tortuosity, copper-or silver-wire appearance, perivascular sheathing, irregularity of lumen and scattered small haemorrhages, and small, sharp-edged deposits without surrounding oedema. (05 Mar 2000) |
| background retinopathy | <ophthalmology, pathology> Early stage of diabetic retinopathy, it usually does not impair vision. Origin: Gr. Pathos = disease (09 Oct 1997) |
| macular retinopathy | Any pathological condition of the macula lutea. Synonym: macular retinopathy. (05 Mar 2000) |
| venous-stasis retinopathy | A uniocular retinopathy associated with occlusion of the central retinal vein; a nonischemic central retinal vein occlusion. (05 Mar 2000) |
| renal retinopathy | Hypertensive retinopathy associated with chronic glomerulonephritis or nephrosclerosis. (05 Mar 2000) |
| central angiospastic retinopathy | Detachment of the sensory retina induced by decreased adhesion between cells of the retinal pigment epithelium which permits plasma from the choriocapillaris to enter subretinal space. Synonym: central angiospastic retinopathy, central serous retinopathy. (05 Mar 2000) |
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