| MD | Doctor of Medicine [Lat. Medicinae Doctor]; magnesium deficiency; main duct; maintenance dose; major... |
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| RFT | respiratory function test; rod-and-frame test; right frontotransverse [fetal position] |
| RMCH | rod monochromacy or monochromatism |
| ROS | reactive oxygen species; review of systems; rod outer segment |
| ROSP | rod outer segment protein |
| rod nuclear cell | <pathology> Immature neutrophils released from the bone marrow reserve in response to acute demand. (18 Nov 1997) |
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| rod outer segment | <ophthalmology, physiology> Major photoreceptor cell of vertebrate retina (about 125 million in a human eye). Columnar cells (about 40m long, 1m diameter) having three distinct regions: a region adjacent to and synapsed with, the neural layer of the retina contains the nucleus and other cytoplasmic organelles, below this is the inner segment, rich in mitochondria, that is connected through a thin neck (in which is located a ciliary body) to the outer segment. The outer segment largely consists of a stack of discs membrane infoldings that are incompletely separated in cones) that are continually replenished near the inner segment and that are shed from the distal end and phagocytosed by the pigmented epithelium. The membranes of the discs are rich in rhodopsin, the pigment that absorbs light. (03 Jul 1999) |
| rod outer segments | The portion of the retinal rod cell between the inner segment and the pigment epithelium layer of the retina. (12 Dec 1998) |
| rod vision | Vision when the eye is dark-adapted. See: dark adaptation, dark-adapted eye. Synonym: night vision, rod vision, scotopia, twilight vision. (05 Mar 2000) |
| withe-rod | <botany> A North American shrub (Viburnum nudum) whose tough osierlike shoots are sometimes used for binding sheaves. Source: Websters Dictionary (01 Mar 1998) |
| harrington rod insertion | <orthopaedics> A procedure that involves fusing together two or more vertebrae in the spine using either bone grafts or metal rods (Harrington rods). This procedure may be used to correct kyphosis or scoliosis. It is also used in those who require spine stabilisation due to vertebral damage from ruptures discs, fractures, osteomyelitis, osteoarthritis or tumour. (27 Sep 1997) |
| enamel rod inclination | The direction of the enamel rods with reference to the outer surface of the enamel of a tooth. (05 Mar 2000) |
| enamel rod sheath | Organic covering of the individual enamel rod. (05 Mar 2000) |
| adiposogenital dystrophy | A disorder characterised primarily by obesity and hypogonadotrophic hypogonadism in adolescent boys; dwarfism is rare, and when present is thought to reflect hypothyroidism. Visual loss, behavioural abnormalities, and diabetes insipidus may occur. Frohlich's syndrome often is used synonymously for this disorder, although the original case involved a pituitary tumour; most cases are thought to result from hypothalamic dysfunction in areas regulating appetite and gonadal development. The most common causes are pituitary and hypothalamic neoplasms. Synonym: adiposis orchica, adiposogenital degeneration, adiposogenital dystrophy, adiposogenital syndrome, hypophysial syndrome, hypothalamic obesity with hypogonadism. Origin: L. Fr. G. Dys-, bad, + trophe, nourishment (05 Mar 2000) |
| adult pseudohypertrophic muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| Barnes' dystrophy | A rare type of muscular dystrophy, in which muscles are often hypertrophic and stronger than normal, but later become weak and atrophic. (05 Mar 2000) |
| Becker's muscular dystrophy | An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (27 Sep 1997) |
| Becker type muscular dystrophy | A muscular dystrophy that has many of the clinical features of Duchenne muscular dystrophy e.g., symmetrical involvement of first the pelvicrural muscles and then the pectoral girdle and proximal upper extremity muscles; pseudohypertrophy, especially of the calf muscles but with a much later age of onset (35-45 years), and more benign course. X-linked inheritance. (05 Mar 2000) |
| Becker type tardive muscular dystrophy | Muscular dystrophy of late onset, often in the second or third decade, with relatively mild course; X-linked recessive inheritance; perhaps allelic with Duchenne's dystrophy, but milder and not a genetic lethal. Compare: Duchenne dystrophy. Synonym: Becker type tardive muscular dystrophy. (05 Mar 2000) |
| benign pseudohypertrophic muscular dystrophy | <neurology> An X-linked inherited disorder characterised by slowly progressive muscle weakness of the legs and pelvis. Other symptoms and findings include increased difficulty walking, intellectual retardation, fatigue and pseudohypertrophy of the calf muscles. (06 Aug 1998) |