| 영문 | hypoplasia | 한글 | 형성저하증 |
|---|---|---|---|
| 설명 | 장기의 불완전한 발달 때문에 성인의 크기에 도달하지 못한 상태. 그 중증도는 무형성보다 가볍다. 개체의 발달과정에서 어떤 원인에 의해 장기조직의 형성이 불완전하게 되는 것을 말한다. 기관 원기는 존재하지만 발육이 불완전하게 끝난 상태이다. 대다수의 경우 원인은 불확실하지만, 원인으로서 생각되는 것으로는 유전, 감염, 영양장애, 내분비장애, 외상, 방사선 등을 들 수 있다. 장기조직이 정상적으로 형성된 뒤 그 체적이 감소해 가는 위축과는 구별된다. |
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| TOF | 1) Tetralogy Of Fallot ? CIx of Corrective Op ... |
|---|---|
| PAGOD | pulmonary hypoplasia-hypoplasia of pulmonary artery-agonadism-omphalocele/diaphragmatic defect-dextr... |
| max | maxilla, maxillary; maximum |
| MMOA | maxillary mandibular odontectomy alveolectomy |
| RME | rapid maxillary expansion; resting metabolic expenditure; right mediolateral episiotomy |
| RME | Rapid maxillary expansion |
|---|---|
| AHC | Adrenal hypoplasia congenita |
| CHH | Cartilage hair hypoplasia |
| FDH | Focal Dermal Hypoplasia |
| PH | Pulmonary hypoplasia |
| parathyroids, hypoplasia of the thymusand | Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands which control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the heart involving the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome. (12 Dec 1998) |
|---|---|
| cartilage-hair hypoplasia | An autosomal recessive form of dwarfism characterised by shortness of the extremities without skull defects, and with sparse, brittle hair of light colour. There is a peculiar, not adequately explained severity in the clinical course of varicella and herpes in such patients. (05 Mar 2000) |
| renal hypoplasia | An abnormally small kidney that is morphologically normal but has either a reduced number of nephrons or smaller nephrons. (05 Mar 2000) |
| right ventricular hypoplasia | A congenital or acquired condition in which there is thinning of the right ventricular myocardium. Synonym: right ventricular hypoplasia. (05 Mar 2000) |
| hypoplasia | <embryology> The incomplete development or underdevelopment of an organ or tissue. Origin: Gr. Plasis = formation (18 Nov 1997) |
| hypoplasia of right ventricle | Failure of development of the right ventricle resulting in its having little muscle and much connective tissue instead of the reverse. (05 Mar 2000) |
| hypoplasia of the thymus and parathyroids | Also known as the digeorge syndrome (dgs), this disorder is characterised by (1) low blood calcium levels (hypocalcaemia) due to underdevelopment (hypoplasia) of the parathyroid glands needed to control calcium; (2) underdevelopment (hypoplasia) of the thymus, an organ behind the breastbone in which lymphocytes mature and multiply; and (3) defects of the outflow tracts from the heart. most cases of dgs are due to a microdeletion in chromosome band 22q11.2. A small number of cases have defects in other chromosomes, notably 10p13. Named after the american paediatric endocrinologist angelo digeorge. Another name for dgs is the third and fourth pharyngeal pouch syndrome (since the faulty structures in dgs are embryologically derived from the third and fourth pharyngeal pouches). (12 Dec 1998) |
| dental enamel hypoplasia | <dentistry> A form of amelogenesis imperfecta characterised by incomplete formation of the dental enamel and transmitted as an x-linked or autosomal dominant trait. It is also associated with vitamin a, c, or d deficiency, infectious disease, prematurity, birth injury, rh incompatibility, trauma, or local infection. Small grooves, pits, and fissures are seen in mild cases, deep horizontal rows of pits in severe cases, or absence of enamel in extreme cases. (12 Dec 1998) |
| optic nerve hypoplasia | Congenitally small optic disk resulting from failure of development of retinal ganglion cells, with a reduced number of axons; visual impairment may be marked. See: de Morsier's syndrome. (05 Mar 2000) |
| thymic hypoplasia | diGeorge syndrome |
| thymus and parathyroids, hypoplasia of | See third and fourth pharyngeal pouch syndrome. (12 Dec 1998) |
| enamel hypoplasia | A developmental disturbance of teeth characterised by deficient or defective enamel matrix formation; may be hereditary, as in amelogenesis imperfecta, or acquired, as encountered in dental fluorosis, local infection, childhood fevers, and congenital syphilis. (05 Mar 2000) |
| focal dermal hypoplasia | A genetic skin disease characterised by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an x-linked dominant trait. (12 Dec 1998) |
| ganglionic branches of maxillary nerve | <anatomy, nerve> The ganglionic branches, two short sensory branches of the maxillary nerve in the pterygopalatine fossa, the fibres of which pass through the pterygopalatine ganglion without synapse. Synonym: radix sensoria ganglii pterygopalatini, rami ganglionici nervi maxillaris, rami ganglionares, nervi pterygopalatini, nervi sphenopalatini, pterygopalatine nerves, sensory root of pterygopalatine ganglion. (05 Mar 2000) |
| maxillary | <anatomy> Pertaining to the maxilla. The irregularly shaped bone that with its fellow forms the upper jaw. Origin: L. Maxillaris (18 Nov 1997) |
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|