| NEC | Necrotizing Entero-Colitis |
|---|---|
| If | nec if necessary |
| NEC | National Electrical Code; necrotizing enterocolitis; neuroendocrine cell; neuroendocrine convertase;... |
| CAV | congenital absence of vagina; congenital adrenal virilism; constant angular velocity; croup-associat... |
| CC | calcaneal-cuboid; calcium cyclamate; cardiac catheterization; cardiac contusion; cardiac cycle; card... |
| primitive palate | In the early embryo, the mesoderm-filled shelf, formed from the medial nasal process, that anteriorly separates the oral cavity below from the primitive nasal cavities above. Synonym: primitive palate. (05 Mar 2000) |
|---|---|
| secondary palate | The posterior portion of the embryonic palate, which forms from the palatal processes of the embryonic maxilla and develops into the hard palate. (05 Mar 2000) |
| soft palate | The muscular part of the roof of the mouth. The soft palate is directly behind the hard palate. It lacks bone and so is soft. (12 Dec 1998) |
| tensor muscle of soft palate | <anatomy> Tensor muscle of soft palate, musculus tensor palati; musculus palatosalpingeus; musculus sphenosalpingostaphylinus; dilator tubae; origin, scaphoid fossa of sphenoid, cartilaginous and membranous part of auditory (eustachian) tube and spine of sphenoid; insertion, posterior border of hard palate and aponeurosis of soft palate; action, tenses the soft palate; contributes to opening of auditory tube; nerve supply, branches of trigeminal nerve through the otic ganglion. Synonym: musculus tensor veli palatini, dilator tubae, musculus palatosalpingeus, musculus sphenosalpingostaphylinus, musculus tensor palati, palatosalpingeus, tensor muscle of soft palate. (05 Mar 2000) |
| elevator muscle of soft palate | <anatomy, muscle> Origin, apex of petrous portion of temporal bone and lower part of cartilaginous auditory (eustachian) tube; insertion, aponeurosis of soft palate; action, raises soft palate; through the expansion of its fleshy belly during contraction, it helps to "push" open the auditory tube; nerve supply, pharyngeal plexus (cranial root of accessory nerve). Synonym: musculus levator veli palatini, elevator muscle of soft palate, levator palati muscle, musculus levator palati, musculus petrostaphylinus. (05 Mar 2000) |
| falling palate | Relaxation or elongation of the uvula. Synonym: falling palate, staphylodialysis, staphyloptosis, uvulaptosis. Origin: uvulo-+ G. Ptosis, a falling (05 Mar 2000) |
| adrenal hyperplasia, congenital | A group of inherited disorders of adrenal steroidogenesis, the physical expression of which varies with the sex of the patient, the severity of the congenital enzyme defect, and the age at which the defect makes its presence felt. The most common form, the simple virilizing form, is due to a 21-hydroxylase deficiency. There is also a salt-losing form (a more complete 21-hydroxylase deficiency), a hypertensive form (11-hydroxylase deficiency), a 17-hydroxylase deficiency form, a desmolase deficiency form, and a 3-beta-hydroxysteroid deficiency form. (12 Dec 1998) |
| anaemia, dyserythropoietic, congenital | A familial disorder characterised by anaemia with multinuclear erythroblasts, karyorrhexis, asynchrony of nuclear and cytoplasmic maturation, and various nuclear abnormalities of bone marrow erythrocyte precursors. Type II is the most common of the 3 types of congenital dyserythropoietic anaemia; it is often referred to as hempas, based on the hereditary erythroblast multinuclearity with positive acidified serum test. (12 Dec 1998) |
| anaemia, haemolytic, congenital | Haemolytic anaemia due to various intrinsic defects of the erythrocyte. (12 Dec 1998) |
| anaemia, haemolytic, congenital nonspherocytic | Any one of a group of congenital haemolytic anaemias in which there is no abnormal haemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. In some cases, pyruvate kinase deficiency has been demonstrated; in other cases, glucose-6-phosphate dehydrogenase deficiency has been demonstrated. (12 Dec 1998) |
| bovine congenital ataxia | An autosomal recessive ataxia seen in several European breeds of cattle. (05 Mar 2000) |
| bullous congenital ichthyosiform erythroderma | Diffusely red, eroded skin at birth, with subsequent scaling, tending to improve in later life, characterised by generalised epidermolytic hyperkeratosis and autosomal dominant inheritance. See: epidermolytic hyperkeratosis. Synonym: generalised epidermolytic hyperkeratosis, ichthyismus hystrix, ichthyosis hystrix. (05 Mar 2000) |
| pain insensitivity, congenital | Absence of sensibility to pain or inability to feel pain. The condition is present at birth. (12 Dec 1998) |
| rubella syndrome, congenital | Transplacental infection of the foetus with rubella usually in the first trimester of pregnancy, as a consequence of maternal infection, resulting in various developmental abnormalities in the newborn infant. They include cardiac and ocular lesions, deafness, microcephaly, mental retardation, and generalised growth retardation. (12 Dec 1998) |
| congenital | <embryology> Existing at and usually before, birth, referring to conditions that are present at birth, regardless of their causation. Origin: L. Congenitus = born together (18 Nov 1997) |