| AE | above-elbow [amputation]; acrodermatitis enteropathica; activation energy; adult erythrocyte; advers... |
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| AEZ | acrodermatitis enteropathica, zinc deficient |
| BCE | basal cell epithelioma; benign childhood epilepsy; bubble chamber equipment |
| BFEC | benign focal epilepsy of childhood |
| BPEC | benign partial epilepsy of childhood; bipolar electrocardiogram |
| papular stomatitis virus of cattle | A poxvirus of the genus Parapoxvirus, reported from North America, Africa and Europe, causing bovine papular stomatitis. Synonym: papular stomatitis virus of cattle. (05 Mar 2000) |
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| papular syphilid | See: follicular syphilid, lenticular syphilid. Papulosquamous syphilid, scaling papules of secondary syphilis. (05 Mar 2000) |
| papular tuberculid | Small asymptomatic lichen papules on the trunk of children with tuberculosis; acid-fast bacilli are not seen in the dermal granulomas. Synonym: acne scrofulosorum, papular scrofuloderma, papular tuberculid. (05 Mar 2000) |
| papular urticaria | A sensitivity reaction to insect bites, especially human and pet fleas, seen mostly in young children as wheals followed by papules on exposed areas. Synonym: lichen urticatus, prurigo infantilis, urticaria papulosa. (05 Mar 2000) |
| miliary papular syphilid | Secondary eruption of small follicular papules, usually appearing as groups of lesions. Synonym: acuminate papular syphilid, lichen syphiliticus, miliary papular syphilid. (05 Mar 2000) |
| flat papular syphilid | Eruption of flattened, dull reddish papules, 5 mm to 1 cm in diameter, occurring in secondary syphilis. Synonym: flat papular syphilid. (05 Mar 2000) |
| avoidant disorder of childhood | A mental disorder occurring in childhood or adolescence characterised by an excessive shrinking away from contact with people who are unfamiliar. Synonym: avoidant disorder of adolescence. (05 Mar 2000) |
| benign childhood epilepsy with centrotemporal spikes | A specific epilepsy syndrome beginning in childhood and remitting in adolescence, characterised by nocturnal simple partial motor seizures or generalised tonic-clonic seizures. EEG shows centrotemporal spikes that are activated by sleep and an otherwise normal EEG background. (05 Mar 2000) |
| recurrent pneumonia in childhood | <radiology> IMMUNE PROBLEMS, immune deficiency, chronic granulomatous disease of childhood, alpha-1 antitrypsin deficiency, ASPIRATION, GE reflux, H-type TE fistula, disorder of swallowing, oesophageal obstruction, UNDERLYING LUNG DISEASE, sequestration, brochopulmonary dysplasia, cystic fibrosis, atopic asthma, bronchiolitis obliterans, sinusitis, bronchiectasis, ciliary dysmotility syndromes, pulmonary foreign body (12 Dec 1998) |
| recurring digital fibromas of childhood | Multiple fibrous flesh-coloured nodules on the extensor aspect of the terminal phalanges of adjacent digits of infants and young children which often recur after attempted excision, do not metastasize, and may spontaneously regress in two to three years; composed of spindle cells containing cytoplasmic inclusions believed to be derived from myofibrils. Synonym: infantile digital fibromatosis. (05 Mar 2000) |
| mental disorders diagnosed in childhood | Those psychiatric disorders usually first diagnosed in infancy, childhood, or adolescence. These disorders can also be first diagnosed during other life stages. (12 Dec 1998) |
| childhood | The period of life between infancy and puberty. (05 Mar 2000) |
| childhood absence epilepsy | A generalised epilepsy syndrome characterised by the onset of absence seizures in childhood, typically at age six or seven years. There is a strong genetic predisposition and girls are affected more often than boys. EEG reveals generalised 3 Hz spike-wave activity on a normal background. Prognosis for remission is good if the patient does not also have generalised tonic-clonic seizures. See: absence. Synonym: petit mal epilepsy, pyknolepsy. (05 Mar 2000) |
| childhood epilepsy with occipital paroxysms | A benign epilepsy syndrome characterised by frequent occipital spikes often activated by eye closure. It has a seizure semiology that includes visual manifestations; not always remitting later in life. (05 Mar 2000) |
| childhood muscular dystrophy | The most common childhood muscular dystrophy, with onset usually before age 6. Characterised by symmetrical weakness and wasting of first the pelvic and crural muscles and then the pectoral and proximal upper extremity muscles; pseudohypertrophy of some muscles, especially the calf; heart involvement; sometimes mild mental retardation; progressive course and early death, usually in adolescence. X-linked inheritance (affects males and transmitted by females). Synonym: childhood muscular dystrophy, Duchenne's disease, pseudohypertrophic muscular dystrophy. (05 Mar 2000) |