| ¿µ¹® | hypothyroidism | ÇÑ±Û | °©»ó»ùÀúÇÏÁõ, °©»ó¼±±â´ÉÀúÇÏÁõ |
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| HEDH | hypohidrotic ectodermal dysplasia-hypothyroidism [syndrome] |
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| HT | Hashimoto thyroiditis; hearing test; hearing threshold; heart; heart transplantation, heart transpla... |
| TRAP | carpal tunnel syndrome, Raynaud phenomenon, aching muscles, proximal muscle weakness [rheumatic diso... |
| CIHS | central infantile hypotonic syndrome |
| CINCA | chronic infantile neurological cutaneous and auricular [syndrome] |
| CH | Congenital Hypothyroidism |
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| CHT | Congenital hypothyroidism |
| EIEE | Early infantile epileptic encephalopathy |
| IHPS | Infantile Hypertrophic Pyloric Stenosis |
| IM | Infantile Myofibromatosis |
| infantile hypothyroidism | <paediatrics> Stunted body growth and mental development appearing in the first years of life resulting the inappropriate development of the thymus gland or inadequate maternal intake of iodine during gestation. (27 Sep 1997) |
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| congenital hypothyroidism | Lack of thyroid secretion. See: infantile hypothyroidism. (05 Mar 2000) |
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| secondary hypothyroidism | Hypothyroidism that arises as a consequence of inadequate thyrotropin secretion by the anterior pituitary gland. (05 Mar 2000) |
| hypothyroidism | <endocrinology> A deficiency of thyroid activity. In adults, it is most common in women and is characterised by decrease in basal metabolic rate, tiredness and lethargy, sensitivity to cold and menstrual disturbances. If untreated, it progresses to full blown myxoedema. In infants, severe hypothyroidism leads to cretinism. In juveniles, the manifestations are intermediate, with less severe mental and developmental retardation and only mild symptoms of the adult form. When due to pituitary deficiency of thyrotropin secretion it is called secondary hypothyroidism. (11 Jan 1998) |
| 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) |
| infantile cataract | A cataract affecting a very young child. (05 Mar 2000) |
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