| IVRT | isovolumic relaxation time |
|---|---|
| NMRD | nuclear magnetic relaxation dispersion |
| PRR | proton relaxation rate; pulse repetition rate |
| RARE | rapid acquisition with relaxation enhancement |
| RRI | recurrent respiratory infection; reflex relaxation index; relative response index |
| infantile progressive spinal muscular atrophy | Transmitted as autosomal recessive on chromosome 5q. Progressive dysfunction of the anterior horn cells in the spinal cord and brainstem cranial nerves with profound weakness and bulbar dysfunction occurring in the first two years of life. Three groups, based on age of clinical onset, are recognised. Synonym: familial spinal muscular atrophy, Hoffmann's muscular atrophy, infantile muscular atrophy, infantile progressive spinal muscular atrophy, progressive infantile spinal muscular atrophy, Werdnig-Hoffmann disease, Werdnig-Hoffmann muscular atrophy. (05 Mar 2000) |
|---|---|
| ophthalmoplegia, chronic progressive external | One of the mitochondrial encephalomyopathies characterised by slowly progressive paralysis of the extraocular muscles. Muscle biopsies disclose the characteristic ragged red fibres and large numbers of mitochondria with deleted DNA. (12 Dec 1998) |
| ovine progressive pneumonia | A chronic, progressive, contagious interstitial pneumonitis of sheep in Europe and the U.S. Caused by a "slow virus" (family Lentiviridae); it is now believed that maedi and visna are two histopathological and clinical manifestations of the same viral infection. Synonym: ovine progressive pneumonia. Origin: Icelandic, dyspnea (05 Mar 2000) |
| traumatic progressive encephalopathy | A chronic progressive brain damage resulting from multiple brain injuries, e.g., dementia pugilistica. (05 Mar 2000) |
| essential progressive atrophy of iris | Progressive atrophy of the iris without inflammatory signs, characterised by patchy loss of all layers of the iris with hole formation, migration of the pupil, degeneration of the corneal endothelium, peripheral anterior synechiae, and secondary glaucoma; usually unilateral, predominantly affecting women in their middle years. (05 Mar 2000) |
| lenticular progressive degeneration | <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) |
| leukoencephalopathy, progressive multifocal | Rare demyelinating disease of the central nervous system which develops in immunocompromised patients secondary to lymphoproliferative disease, immunosuppressive therapy, autoimmune disorders, or aids. It is caused by the jc virus, a polyomavirus. (12 Dec 1998) |
| abdominal external oblique muscle | <anatomy, muscle> Origin, fifth to twelfth ribs; insertion, anterior half of lateral lip of iliac crest, inguinal ligament, and anterior layer of the rectus sheath; action, diminishes capacity of abdomen, draws thorax downward; nerve supply, thoracoabdominal nerves. Synonym: musculus obliquus externus abdominis, abdominal external oblique muscle. (05 Mar 2000) |
| abdominal internal oblique muscle | <anatomy, muscle> Origin, iliac fascia deep to lateral part of inguinal ligament, anterior half of crest of ilium, and lumbar fascia; insertion, tenth to twelfth ribs and sheath of rectus; some of the fibres from inguinal ligament terminate in the conjoint tendon; action, diminishes capacity of abdomen, flexes lumbar vertebral column (bends thorax forward); nerve supply, lower thoracic. Synonym: musculus obliquus internus abdominis, abdominal internal oblique muscle. (05 Mar 2000) |
| abdominal muscle deficiency syndrome | <syndrome> Congenital absence (partial or complete) of abdominal muscles, in which the outline of the intestines is visible through the protruding abdominal wall; in males, genitourinary anomalies (urinary tract dilation and cryptorchidism) are also found; genetics unclear. (05 Mar 2000) |
| abductor digiti minimi muscle of foot | Origin, lateral and medial processes of calcanean tuberosity; insertion, lateral side of proximal phalanx of fifth toe; action, abducts and flexes little toe; nerve supply, lateral plantar nerve. Synonym: musculus abductor digiti minimi pedis, abductor muscle of little toe, musculus abductor digiti quinti. (05 Mar 2000) |
| abductor digiti minimi muscle of hand | Origin, pisiform bone and pisohamate ligament; insertion, medial side of base of proximal phalanx of the little finger; action, abducts and flexes little finger; nerve supply, ulnar. Synonym: musculus abductor digiti minimi manus, abductor muscle of little finger, musculus abductor digiti quinti. (05 Mar 2000) |
| abductor muscle | <anatomy> Any muscle used to pull a body part away from the midline of the body. For example, the abductor leg muscles serve to spread the legs. The opposite of abductor is adductor. (12 Dec 1998) |
| abductor muscle of great toe | <anatomy, muscle> Origin, medial process of calcaneal tuberosity, flexor retinaculum, and plantar aponeurosis; insertion, medial side of proximal phalanx of great toe; action, abducts great toe; nerve supply, medial plantar. Synonym: musculus abductor hallucis, abductor muscle of great toe. (05 Mar 2000) |
| abductor muscle of little finger | Origin, pisiform bone and pisohamate ligament; insertion, medial side of base of proximal phalanx of the little finger; action, abducts and flexes little finger; nerve supply, ulnar. Synonym: musculus abductor digiti minimi manus, abductor muscle of little finger, musculus abductor digiti quinti. (05 Mar 2000) |