| ¿µ¹® | infancy | ÇÑ±Û | ¿µ¾Æ±â, À¯¾Æ±â |
|---|---|---|---|
| ¼³¸í | ½Å»ý¾Æ¸¦ Æ÷ÇÔÇØ Ãâ»ý ÈÄ 1³â±îÁöÀÇ ±â°£. ½Åü¹ßÀ° ¹× ¿îµ¿±â´ÉÀÇ ¹ß´ÞÀÌ ¸Å¿ì Ȱ¹ßÇÑ ½Ã±â·Î¼ ½Å»ý¾Æ ¶§ºÎÅÍ °è¼ÓÇØ¼ ȯ°æ¿¡ ÀûÀÀÇØ °¡´Â Áß¿äÇÑ ½Ã±âÀÌ´Ù. Á¥´Ï°¡ ³ª¿À¸ç ¸é¿ª±â´ÉÀÇ È°¼ºÈ, ¹Ý»çÀÇ ¼Ò½Ç°ú ¼öÀǿÀÇ ¹ß´Þ, °¨°¢(½Ã°¢, û°¢, Ã˰¢) ±â´ÉÀÇ ¹ß´Þ, üÁß°ú ŰÀÇ Áõ°¡¸¦ È®ÀÎÇÒ ¼ö ÀÖ´Ù. üÁßÀº 3°³¿ù¿¡ 2¹è, 1³â¿£ 3¹è°¡ µÇ¸ç, Ű´Â 1³â¿¡ ¾à 27cm ÀÚ¶õ´Ù. 2. ¸¸ 1¼¼ºÎÅÍ 6¼¼±îÁöÀÇ ¾î¸° ½Ã±â, ÀÚ±âÁ߽ɼº, Á¤¼¼º, ±¸Ã¼¼ºÀÌ ³ªÅ¸³ª¸ç ¸¸ 3¼¼±îÁöÀÇ Àü±â¿¡´Â ÀÏ»ó¾îÀÇ ½Àµæ, »ýȰ ½À°üÀÇ È®¸³ µûÀ§°¡ ÀÌ·ç¾îÁö°í Èı⿡´Â °³¼ºÀÌ ¶Ñ·ÇÇÏ¿©Áø´Ù. |
||
| IACI | idiopathic arterial calcification of infancy |
|---|---|
| PHHI | persistent hyperinsulinemic hypoglycemia of infancy |
| SMEI | severe myoclonic epilepsy of infancy |
| SUDI | sudden unexpected death in infancy |
| THI | transient hypogammaglobulinemia of infancy |
| MNTI | Melanotic neuroectodermal tumor of infancy |
|---|---|
| PHHI | Persistent hyperinsulinaemic hypoglycaemia of infancy |
| SMEI | Severe myoclonic epilepsy in infancy |
| ICP | infancy childhood puberty |
| acropustulosis | Pustular eruptions of the hands and feet, often a form of psoriasis. Origin: acro-+ pustulosis Infantile acropustulosis, a cyclically recurrent papulopustular and crusting pruritic eruption, usually in black children, appearing soon after birth to 10 months; remission occurs at about 2 years of age. (05 Mar 2000) |
|---|---|
| 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) |
| 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) |
| 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) |
| 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) |
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|
Á¦Ç°¸í |
ÆÇ¸Å»ç |
º¸ÇèÄÚµå | ¼ººÐ/ÇÔ·® | ±¸ºÐ/º¸Çè±Þ¿© |
|---|