| ¿µ¹® | infancy | ÇÑ±Û | ¿µ¾Æ±â, À¯¾Æ±â |
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| ¿µ¹® | transient ischemic attack(TIA) | ÇÑ±Û | Àϰú¼ºÇãÇ÷¹ßÀÛ |
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| ¼³¸í | ³úÇ÷°ü Æó¼â¿¡ ÀÇÇÑ Àϰú¼ºÀÇ ½Ç½Å, µÎÅë, ½Ã·Â»ó½Ç µîÀÇ Áõ¼¼¸¦ º¸ÀÌ´Â »óÅ·Π24½Ã°£ À̳»¿¡ ¸ðµç Áõ»óÀÌ È¸º¹µÇ´Â °æ¿ì¸¦ ¸»ÇÑ´Ù. ÈÄ¿¡ ¿µ±¸ÀûÀÎ ³úÇãÇ÷ Áï ³ú°æ»öÁõÀÌ ¿Ã °¡´É¼ºÀÌ ¸Å¿ì ³ô¾ÆÁø´Ù. |
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| THI | transient hypogammaglobulinemia of infancy |
|---|---|
| IACI | idiopathic arterial calcification of infancy |
| PHHI | persistent hyperinsulinemic hypoglycemia of infancy |
| SMEI | severe myoclonic epilepsy of infancy |
| SUDI | sudden unexpected death in infancy |
| MNTI | Melanotic neuroectodermal tumor of infancy |
|---|---|
| PHHI | Persistent hyperinsulinaemic hypoglycaemia of infancy |
| SMEI | Severe myoclonic epilepsy in infancy |
| ICP | infancy childhood puberty |
| HITS | High Intensity Transient Signals |
| transient hypogammaglobulinaemia of infancy | A type of primary immunodeficiency that occurs in infants of both sexes, usually before the sixth month of life, probably resulting from immaturity of lymphoid tissue. Synonym: transient agammaglobulinaemia. (05 Mar 2000) |
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| acquired hypogammaglobulinaemia | Heterogeneous group of immunodeficiency syndromes characterised by hypogammaglobulinaemia of most isotypes, variable B-cell defects, and the presence of recurrent bacterial infections. (12 Dec 1998) |
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| melanotic neuroectodermal tumour of infancy | A benign neoplasm of neuroectodermal origin that most often involves the anterior maxilla of infants in the first year of life. It presents clinically as a rapidly growing blue-black lesion producing a destructive radiolucency; histologically, it is characterised by small round undifferentiated tumour cells interspersed with larger polyhedral melanin-producing cells arranged in an alveolar configuration. Synonym: melanoameloblastoma, pigmented ameloblastoma, pigmented epulis, progonoma of jaw, retinal anlage tumour. (05 Mar 2000) |
| primary hypogammaglobulinaemia | Hypogammaglobulinaemia due to a primary immunodeficiency of immunoglobulin-forming cells (B-lymphocytes). (05 Mar 2000) |
| X-linked hypogammaglobulinaemia | A congenital, X-linked recessive, primary immunodeficiency characterised by decreased numbers (or absence) of circulating B-lymphocytes with corresponding decrease in immunoglobulins of the five classes; associated with marked susceptibility to infection by pyogenic bacteria (notably, pneumococci and Haemophilus influenzae) beginning after loss of maternal antibodies. X-linked hypogammaglobulinaemia with growth hormone deficiency, hypogammaglobulinaemia combined with a reduced number of B-cells; characterised by short stature, delayed puberty, and recurrent infections. (05 Mar 2000) |
| secondary hypogammaglobulinaemia | Immunodeficiency in which there is no evident defect in the lymphoid tissues, but rather hypercatabolism or loss of immunoglobulins such as occurs in familial idiopathic hypercatabolic hypoproteinaemia or in defects associated with the nephrotic syndrome. Synonym: secondary agammaglobulinaemia, secondary antibody deficiency, secondary hypogammaglobulinaemia. (05 Mar 2000) |
| hypogammaglobulinaemia | <biochemistry> Syndromes in humans and other vertebrates in which the immunoglobulin level is depressed below the normal range. Congenital, chronic and transient types are known. Origin: Gr. Haima = blood (11 Jan 1998) |
| spongy degeneration of infancy | Autosomal recessive degenerative disease of infancy; mostly in Jewish infants; onset typically within first 3-4 months of birth, consisting of blindness, psychomotor regression, enlarged head, optic atrophy, hypotonia, spasticity, increased N-acetylaspartic acid urinary excretion. MRI shows enlarged brain, decreased attenuation of cerebral and cerebellar white matter, and normal ventricles. Pathologically, there is increased brain volume and weight, and spongy degeneration in the subcortical white matter. See: leukodystrophy. Synonym: Canavan's sclerosis, Canavan-van Bogaert-Bertrand disease, spongy degeneration of infancy. (05 Mar 2000) |
| diencephalic syndrome of infancy | <paediatrics> Profound emaciation after initial normal growth, locomotor hyperactivity and euphoria, usually with skin pallor, hypotension and hypoglycaemia. It is usually due to neoplasm involving the anterior hypothalamus. (05 Mar 2000) |
| infancy | Babyhood; the earliest period of extrauterine life; roughly, the first year of life. (05 Mar 2000) |
| fibrous hamartoma of infancy | A tumour appearing usually in the upper arm or shoulder in the first two years of life and consisting of cellular fibrous tissue infiltrating the subcutis. (05 Mar 2000) |
| cerebral ischemia, transient | Nonconvulsive, reversible, focal neurologic deficits lasting minutes up to about 24 hours, resulting mainly from arteriosclerosis, emboli, or hypertensive episodes. (12 Dec 1998) |
| transient | 1. Short-lived; passing; not permanent; said of a disease or an attack. 2. A short-lived cardiac sound having little duration (less than 0.12 second) as distinct from a murmur; e.g., first, second, third, and fourth heart sounds, clicks, and opening snaps. Origin: L. Transeo, pres. P. Transiens, to cross over (05 Mar 2000) |
| transient acantholytic dermatosis | A pruritic papular eruption, with histologic suprabasal acantholysis, of the chest, with scattered lesions of the back and lateral aspects of the extremities, lasting from a few weeks to several months; seen predominantly in males over 40. Synonym: Grover's disease. (05 Mar 2000) |
| transient agammaglobulinaemia | A type of primary immunodeficiency that occurs in infants of both sexes, usually before the sixth month of life, probably resulting from immaturity of lymphoid tissue. Synonym: transient agammaglobulinaemia. (05 Mar 2000) |
| transient albuminuria | Albuminuria of a temporary or short-lived nature. (05 Mar 2000) |
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