| ¿µ¹® | hypoplasia | ÇÑ±Û | Çü¼ºÀúÇÏÁõ |
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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... |
| TS | Takayasu syndrome; Tay-Sachs; temperature sensitivity; temperature, skin; temporal stem; tensile str... |
| UT | total unsharpness; Ullrich-Turner [syndrome]; Unna-Thost [syndrome]; untested; untreated; urinary tr... |
| UTS | Ullrich-Turner syndrome; ulnar tunnel syndrome; ultimate tensile strength |
| TS | Turner Syndrome |
|---|---|
| UTS | Ullrich-Turner Syndrome |
| AHC | Adrenal hypoplasia congenita |
| CHH | Cartilage hair hypoplasia |
| FDH | Focal Dermal 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) |
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| 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) |
| Parsonage-Turner syndrome | A neurological disorder, of unknown cause, characterised by the sudden onset of severe pain, usually about the shoulder and often beginning at night, soon followed by weakness and wasting of various forequarter muscles, particularly shoulder girdle muscles; both sporadic and familial in occurrence with the former much more common; often preceded by some antecedent event, such as an upper respiratory infection, hospitalization, vaccination, or non-specific trauma; usually attributed to a brachial plexus lesion, because the nerve fibres involed are most often derived from the upper trunk, but actually multiple proximal mononeuropathies. Synonym: acute brachial radiculitis, brachial plexitis, brachial plexus neuropathy, Parsonage-Turner syndrome, shoulder-girdle syndrome. (05 Mar 2000) |
| Grey Turner's sign | <clinical sign> Local areas of discoloration about the umbilicus and in the region of the loins, in acute haemorrhagic pancreatitis and other causes of retroperitoneal haemorrhage. (05 Mar 2000) |
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