| IAFI | infantile amaurotic familial idiocy |
|---|---|
| IBSN | infantile bilateral striated necrosis |
| ICP | incubation period; indwelling catheter program; infantile cerebral palsy; infection-control practiti... |
| IDBS | infantile diffuse brain sclerosis |
| IGA | infantile genetic agranulocytosis |
| temporomandibular articulation | <anatomy, dentistry> The joint that connects the lower jaw to the skull. (12 Jan 1998) |
|---|---|
| tibiofibular articulation | The plane synovial joint between the lateral condyle of the tibia and the head of the fibula. Synonym: articulatio tibiofibularis, superior tibial articulation, superior tibiofibular joint, tibiofibular articulation. (05 Mar 2000) |
| transverse tarsal articulation | The synovial joints between the talus and navicular bone medially and the calcaneus and navicular bones laterally which act as a unit in allowing the front of the foot to pivot relative to the back of the foot about the longitudinal axis of the foot, contributing to the total inversion and eversion movements. Synonym: articulatio tarsi transversa, Chopart's joint, midtarsal joint, transverse tarsal articulation. (05 Mar 2000) |
| trochoid articulation | A synovial joint in which a section of a cylinder of one bone fits into a corresponding cavity on the other, as in the proximal radioulnar joint. Synonym: articulatio trochoidea, helicoid ginglymus, lateral ginglymus, rotary joint, rotatory joint, trochoid articulation, trochoid joint. (05 Mar 2000) |
| aggressive infantile fibromatosis | A childhood counterpart of abdominal or extra-abdominal desmoid tumours, characterised by firm subcutaneous nodules that grow rapidly in any part of the body that invade locally and recur but do not metastasize. (05 Mar 2000) |
| autism, infantile | A syndrome beginning in infancy and characterised by a lack of responsiveness to other people, gross impairment in verbal and nonverbal communication skills, and bizarre responses to the environment. (12 Dec 1998) |
| progressive infantile spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
| spasms, infantile | Primary generalised epileptic seizures occurring in infants between birth and twelve months of age consisting of brief synchronous contractions of the neck, torso, and both arms. These seizures often occur in infants with underlying neurologic diseases. The prognosis for these infants is grave, with approximately ninety percent developing mental retardation in addition to their seizures. The eeg has a typical hypsarrhythmia pattern. The spasms and hypsarrhythmia have a tendency to disappear over the first three to five years of life, only to be replaced by other forms of generalised seizures. Infantile spasms sometimes respond to valproic acid or acth. (12 Dec 1998) |
| supravalvar aortic stenosis-infantile hypercalcaemia syndrome | <syndrome> Supravalvar aortic stenosis associated with elfin facies, mental retardation, and hypercalcaemia; usually sporadic; perhaps an irregular dominant trait. (05 Mar 2000) |
| diffuse infantile familial sclerosis | <radiology> Dysmyelinating disease, autosomal recessive, usually presents by 1 yr, specific enzyme deficiency identified, rapid spontaneous nystagmus, poikilothermia Synonym: Krabbe leukodystrophy (12 Dec 1998) |
| infantile | Pertaining to an infant or to infancy. Origin: L. Infantilis (18 Nov 1997) |
| infantile acute haemorrhagic oedema of the skin | A generally benign form of cutaneous vasculitis, characterised by ecchymotic purpura, often in a cockade pattern, and inflammatory oedema in infants. (05 Mar 2000) |
| infantile autism | A severe emotional disturbance of childhood characterised by qualitative impairment in reciprocal social interaction and in communication, language, and social development. Synonym: autistic disorder, childhood schizophrenia, early infantile autism, Kanner's syndrome. (05 Mar 2000) |
| infantile beriberi | Beriberi appearing in a breast-fed infants whose mother has beriberi due to thiamin deficiency. It is mainly the "wet" form of beriberi, characterised by heart failure with marked peripheral oedema (which is otherwise unusual in heart failure in infancy). An often fatal disease, acute in onset, which was formerly common in the Far Eastern countries where rice is consumed; reversible with thiamin. (05 Mar 2000) |
| infantile brain tumours | <radiology> Can be present at birth: choroid plexus papilloma, medulloblastoma, craniopharyngioma, ependymoma, astrocytoma, teratoma (12 Dec 1998) |