| enamel nodule | A developmental anomaly in which there is a small nodule of enamel below the cementoenamel junction, usually at the bifurcation of molar teeth. Synonym: enamel drop, enamel nodule, enamel pearl. (05 Mar 2000) |
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| enamel organ | Epithelial cells surrounding the dental papilla and differentiated into three layers: the inner enamel epithelium, consisting of ameloblasts which eventually form the enamel, and the enamel pulp and external enamel epithelium, both of which atrophy and disappear before and upon eruption of the tooth, respectively. (12 Dec 1998) |
| enamel pearl | A developmental anomaly in which there is a small nodule of enamel below the cementoenamel junction, usually at the bifurcation of molar teeth. Synonym: enamel drop, enamel nodule, enamel pearl. (05 Mar 2000) |
| enamel prisms | The calcified, microscopic rods radiating from the surface of the dentin, forming the substance of the enamel of a tooth. Synonym: enamel fibres, enamel prisms, enamel rods. (05 Mar 2000) |
| enamel projection | Extension of enamel into furcation. (05 Mar 2000) |
| enamel pulp | A layer of stellate cells in the enamel organ. (05 Mar 2000) |
| enamel rod inclination | The direction of the enamel rods with reference to the outer surface of the enamel of a tooth. (05 Mar 2000) |
| enamel rods | The calcified, microscopic rods radiating from the surface of the dentin, forming the substance of the enamel of a tooth. Synonym: enamel fibres, enamel prisms, enamel rods. (05 Mar 2000) |
| enamel rod sheath | Organic covering of the individual enamel rod. (05 Mar 2000) |
| enamel tuft | A group of structures representing defects in tooth mineralization that extend from the dentino-enamel junction into the enamel to about one-half its thickness. (05 Mar 2000) |
| enamel wall | In dentistry, the part of the wall of a cavity consisting of enamel. (05 Mar 2000) |
| Albright's hereditary osteodystrophy | An inherited form of hyperparathyroidism associated with ectopic calcification and ossification and skeletal defects, notably the small fourth metacarpals, but intelligence is normal. There are dominant, recessive and X-linked forms. See: pseudohypoparathyroidism. Synonym: Albright's syndrome. (05 Mar 2000) |
| angioedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioneurotic oedema. (12 Dec 1998) |
| angioneurotic oedema, hereditary | A genetic form of angioedema. (Angioedema is also referred to as Quinke's disease.) Persons with it are born lacking an inhibitor protein (called C1 esterase inhibitor) that normally prevents activation of a cascade of proteins leading to the swelling of angioedema. Patients can develop recurrent attacks of swollen tissues, pain in the abdomen, and swelling of the voice box (larynx) which can compromise breathing. The diagnosis is suspected with a history of recurrent angioedema. It is confirmed by finding abnormally low levels of C1 esterase inhibitor in the blood. Treatment options include antihistamines and male steroids (androgens) that can also prevent the recurrent attacks. Also called hereditary angioedema. (12 Dec 1998) |
| canine hereditary blindness | An autosomal dominant condition seen in dogs of the collie and several other breeds. (05 Mar 2000) |