CCHS |
congenital central hypoventilation syndrome |
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CCVM |
congenital cardiovascular malformation |
CDA |
Canadian Dental Association; Certified Dental Assistant; chenodeoxycholic acid; ciliary dyskinesia a... |
CEP |
chronic eosinophilic pneumonia; chronic erythropoietic porphyria; congenital erythropoietic porphyri... |
CET |
capital expenditure threshold; congenital eyelid tetrad |
congenital nevus |
A melanocytic nevus that is visible at birth, is often larger than an acquired nevus, and more frequently involves deeper structures. (05 Mar 2000) |
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congenital nonregenerative anaemia |
Congenital nonregenerative, familial hypoplastic, or pure red cell anaemia; erythrogenesis imperfecta; Diamond-Blackfan syndrome; autosomal recessive normocytic normochromic anaemia resulting from congenital hypoplasia of the bone marrow, which is grossly deficient in erythroid precursors while other elements are normal; anaemia is progressive and severe, but leukocyte and platelet counts are normal or slightly reduced; survival of transfused erythrocytes is normal; minor congenital anomalies are found in some patients. Synonym: congenital nonregenerative anaemia, Diamond-Blackfan anaemia, Diamond-Blackfan syndrome, erythrogenesis imperfecta, familial hypoplastic anaemia, pure red cell anaemia. (05 Mar 2000) |
congenital nystagmus |
Nystagmus present at birth or caused by lesions sustained in utero or at the time of birth, inherited nystagmus, usually X-linked, without associated neurologic lesions and nonprogressive; all three patterns of mendelian inheritance may occur: autosomal dominant, autosomal recessive,, the nystagmus associated with albinism, achromatopsia, and hypoplasia of the macula. (05 Mar 2000) |
congenital pancytopenia |
<haematology> A rare inherited type of aplastic anaemia which carries an increased risk to the patient of developing leukaemia. May be treated by bone marrow transplant. Origin: Gr. Haima = blood (13 Nov 1997) |
congenital paramyotonia |
Paramyotonia congenita, a nonprogressive myotonia induced by exposure of muscles to cold; there are episodes of intermittent flaccid paralysis, but no atrophy or hypertrophy of muscles; autosomal dominant inheritance. There is a variant autosomal dominant form in which cold is not a provoking factor. Synonym: Eulenburg's disease. (05 Mar 2000) |
congenital pneumonia |
Pneumonia in the newborn, infection being contracted prenatally. (05 Mar 2000) |
congenital protein C or s deficiency |
This inherited disorder of blood coagulation is characterised by a deficiency of vitamin K dependent plasma proteins (C and s) that are naturally occurring anticoagulants. This disorder results in an increased risk of blood clot formation within the circulatory system. (27 Sep 1997) |
congenital pulmonary arteriovenous fistula |
Abnormal congenital communication between pulmonary arteries and veins usually found in the lung parenchyma. (05 Mar 2000) |
congenital pyloric stenosis |
<radiology> Not seen until 3 weeks, projectile vomiting, palpable olive in RUQ/epigastrium (12 Dec 1998) |
congenital renal cysts |
<radiology> Congenital solitary cyst, multilocular cyst, multicystic disease (renal dysplasia), polycystic disease, autosomal-recessive (childhood) form, autosomal-dominant (adult) form, medullary sponge kidney, medulary cystic disease see also: Potter syndrome (12 Dec 1998) |
congenital renal osteodystrophy |
<radiology> Tubular form of renal osteodystrophy, vitamin D-resistant rickets, Fanconi syndrome, renal tubular acidosis (12 Dec 1998) |
congenital rubella syndrome |
<syndrome> Foetal infection with rubella virus during the first trimester of pregnancy resulting in a series of congenital abnormalities including heart disease, deafness, and blindness. (05 Mar 2000) |
congenital sebaceous hyperplasia |
Misnomer for nevus sebaceus. (05 Mar 2000) |
congenital severe combined immunodeficiency |
Disease, one form of which is caused by the lack of a transcription factor required for expression of HLA class II genes. (18 Nov 1997) |
congenital sinus tumour |
<radiology> Midline depression or tract, lined with stratified squamous epithelium, most common sites: lumbosacral area, occiput, epidermoid or dermoid cyst anywhere along tract (12 Dec 1998) |
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congenital nevus
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pigmented lesion in the dermis that is present at birth
출처: www.beautysurg.com/resources/glossary_c.html
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congenital erythropoietic porphyria
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Congenital erythropoietic porphyria is a rare type of porphyria that mainly affects the skin. The disorder results from low levels of the enzyme responsible for the fourth step in heme production. Heme is a vital molecule for all of the body's organs. It is a component of hemoglobin, the molecule that carries oxygen in the blood. Congenital erythropoietic porphyria is a subtype of porphyria. Congenital erythropoietic porphyria causes the skin to be overly sensitive to sunlight. ...
출처: goldbamboo.com/glossary-1c-v1-u-all1.html
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congenital anomaly
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An abnormality present at birth.
출처: www.health.qld.gov.au/qldheartkids/glossarycd.asp
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congenital
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Any trait present at birth, whether the result of a genetic or nongenetic factor. Source : Human Genome Project Information
출처: www.genomecanada.ca/GCglossaire/glossaire/index.as...
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congenital
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Existing at or dating from birth; acquired during development in the uterus and not through heredity.
출처: www.colonrectal.org/patientinfo/definitions/defini...
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