| BTR | Bezold-type reflex; biceps tendon reflex |
|---|---|
| CR | calculation rate; calculus removed; calorie-restricted; cardiac rehabilitation; cardiac resuscitatio... |
| MSR | macrophage scavenger receptor; Member of the Society of Radiographers; monosynaptic reflex; muscle s... |
| PR | by way of the rectum [Lat. per rectum]; far point [of accommodation] [Lat. punctum remotum]; palindr... |
| RAPD | Relative Afferent Pupillary Defect |
| Westphal's pseudosclerosis | <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure. Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common. Inheritance: autosomal recessive. (27 Sep 1997) |
|---|---|
| Westphal's sign | <clinical sign> Abolition of the patellar tendon reflex, in tabes and certain other diseases of the spinal cord, and occasionally also in brain disease. Synonym: Erb sign, Westphal's phenomenon, Westphal's sign, Westphal-Erb sign. (05 Mar 2000) |
| Westphal-Strumpell pseudosclerosis | <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure. Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common. Inheritance: autosomal recessive. (27 Sep 1997) |
| Strumpell-Westphal disease | <gastroenterology, neurology> An inherited (autosomal recessive) disorder where there is excessive quantities of copper in the tissues, particularly the liver and central nervous system. Wilson's disease causes the body to absorb and retain copper. The copper deposits in the liver, brain, kidneys and eyes. Complications include dementia and liver failure. Symptoms include jaundice, vomiting, tremors, weakness and slow stiff movements. Blood tests show serum ceruloplasmin is low. Medications are given to remove the excess copper from the body. Even with life-long treatment, disabling (and life-threatening) side effects are common. Inheritance: autosomal recessive. (27 Sep 1997) |
| Edinger-Westphal nucleus | A small group of preganglionic parasympathetic motor neurons in the midline near the rostral pole of the oculomotor nucleus of the midbrain; the axons of these motor neurons leave the brain with the oculomotor nerve and synapse on the cells of the ciliary ganglion which in turn innervate the sphincter muscle of the pupil and ciliary muscle. Destruction of this nucleus or its efferent fibres causes maximal paralytic dilation of the pupil; also demonstrated to project fibres to lower levels of the brainstem and all spinal levels. (05 Mar 2000) |
| Erb-Westphal sign | <clinical sign> Abolition of the patellar tendon reflex, in tabes and certain other diseases of the spinal cord, and occasionally also in brain disease. Synonym: Erb sign, Westphal's phenomenon, Westphal's sign, Westphal-Erb sign. (05 Mar 2000) |
| relative afferent pupillary defect | An asymmetry of the pupillomotor input between the two eyes; tested by alternating the light from one eye to the other and comparing the direct light reactions. (05 Mar 2000) |
| pupillary | 1. Of or pertaining to a pupil or ward. 2. <anatomy> Of or pertaining to the pupil of the eye. Origin: L. Pupillaris: cf. F.pupillaire. See Pupil. Source: Websters Dictionary (01 Mar 1998) |
| pupillary axis | A line perpendicular to the surface of the cornea, passing through the centre of the pupil; the "direction of gaze." (05 Mar 2000) |
| pupillary block glaucoma | Glaucoma secondary to failure of the aqueous humor to pass through the pupil to the anterior chamber. (05 Mar 2000) |
| pupillary border of iris | The inner border of the iris that forms the edge of the pupil. Synonym: margo pupillaris iridis, pupillary margin of iris. (05 Mar 2000) |
| pupillary dilation | <ophthalmology> The action of stretching or enlarging the pupil for example by atropine. (18 Nov 1997) |
| pupillary distance | The distance between the centre of each pupil; the major reference points in measuring for fitting of spectacle frames and lenses. (05 Mar 2000) |
| pupillary functions, abnormal | Conditions in which the pupil does not react normally to dilation and constriction. Signs of pupillary abnormalities originate from the pupil's shape, position, and response to stimulation. (12 Dec 1998) |
| pupillary light-near dissociation | A stronger near pupil response than light response; due to weak pupillomotor input, Argyll Robertson pupil, dorsal midbrain syndrome, or to misdirection of ciliary muscle fibres into the iris sphincter. Synonym: light-near dissociation. (05 Mar 2000) |