| PCD | pacer-cardioverter-defibrillator; papillary collecting duct; paraneoplastic cerebellar degeneration;... |
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| PSS | painful shoulder syndrome; physiologic saline solution; porcine stress syndrome; primary Sjogren syn... |
| DEF | decayed primary teeth requiring filling, decayed primary teeth requiring extraction, and primary tee... |
| PA | panic attack; pantothenic acid; paralysis agitans; paranoia; passive aggressive; pathology; patient'... |
| PCC | Pasteur Culture Collection; percutaneous cecostomy; pheochromocytoma; phosphate carrier compound; pl... |
| PCD | Paraneoplastic cerebellar degeneration |
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| prcd | Progressive rod-cone degeneration |
| PPA | Primary Progressive Aphasia |
| PP | primary progressive |
| primary SS | Primary Sjogren's syndrome |
primary's area
| primary progressive cerebellar degeneration | A familial ataxic condition related to cerebellar degeneration. (05 Mar 2000) |
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| progressive cerebellar tremor | <syndrome> An intention tremor beginning in one extremity, gradually increasing in intensity, and subsequently involving other parts of the body. Synonym: progressive cerebellar tremor. Facial paralysis, otalgia, and herpes zoster resulting from viral infection of the seventh cranial nerve and geniculate ganglion, a form of juvenile paralysis agitans associated with primary atrophy of the pallidal system. Synonym: paleostriatal syndrome, pallidal syndrome. Synonym: Ramsay Hunt's syndrome. (05 Mar 2000) |
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| 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) |
| aphasia, primary progressive | A type of aphasia appearing gradually and gradually worsening without any major change in other cognitive functions. It is regarded by some authors as a syndrome which may be due to various degenerative diseases of the cerebral cortex (notably alzheimer disease, owing to its frequency), while others see in it an autonomous disease related to a neuropathological process that is distinct from the main degenerative dementias. The principal clinical peculiarity of primary progressive aphasia is that it spares the patient's autonomy for a long time, but ultimately turns into global dementia. (12 Dec 1998) |
| primary neuronal degeneration | <disease> A progressive, neurodegenerative disease characterised by loss of function and death of nerve cells in several areas of the brain leading to loss of cognitive function such as memory and language. The cause of nerve cell death is unknown but the cells are recognised by the appearance of unusual helical protein filaments in the nerve cells (neurofibrillary tangles) and by degeneration in cortical regions of brain, especially frontal and temporal lobes. Alzheimer's disease is the most common cause of dementia. (22 May 1997) |
| primary pigmentary degeneration of retina | A hereditary disorder of the retina mainly affecting photoreceptors and retinal pigment epithelium; a miscellaneous category including Friedreich's ataxia, Refsum's disease, and abetalipoproteinaemia. Synonym: primary pigmentary degeneration of retina. (05 Mar 2000) |
| anterior cerebellar notch | A wide, shallow notch on the anterior surface of the cerebellum occupied laterally by the superior cerebellar peduncles and the inferior quadrigeminal bodies medially. Synonym: anterior notch of cerebellum, incisura cerebelli anterior, semilunar notch. (05 Mar 2000) |
| anterior inferior cerebellar artery | <anatomy, artery> Origin, basilar; distribution, lower surface of lateral lobes of cerebellum, choroid plexus in cerebellopontine angle; anastomoses, posterior inferior cerebellar; usual source of labyrinthine artery. Synonym: arteria cerebelli inferior anterior. (05 Mar 2000) |
| ganglionic layer of cerebellar cortex | The layer of Purkinje cells between the molecular and granular layers of the cerebellar cortex. Synonym: stratum neuronorum piriformium, ganglionic layer of cerebellar cortex, layer of piriform neurons, Purkinje's layer, stratum gangliosum cerebelli. (05 Mar 2000) |
| cerebellar | <anatomy> Pertaining to the cerebellum. (18 Nov 1997) |
| cerebellar arteries | An artery related to and supplying the cerebellum. See: anterior inferior cerebellar artery, posterior inferior cerebellar artery, superior cerebellar artery. (05 Mar 2000) |
| cerebellar astrocytoma | <oncology, tumour> This primary brain tumour of the cerebellum accounts for 10 to 30% of brain tumours in children. The are usually slow growing and benign. Symptoms include gait problems, clumsiness, headache and vomiting. Treatment often involves a combination of surgery, radiation therapy and chemotherapy. (27 Sep 1997) |
| cerebellar ataxia | Loss of muscle coordination caused by disorders of the cerebellum. (05 Mar 2000) |
| cerebellar atrophy | A degeneration of the cerebellum, particularly the Purkinje cells, as the result of abiotrophy or of toxic agents, as in alcoholism. (05 Mar 2000) |
| cerebellar cortex | The thin gray surface layer of the cerebellum, consisting of an outer molecular layer or stratum moleculare, a single layer of Purkinje cells (the ganglionic layer), and an inner granular layer or stratum granulosum. Synonym: cortex cerebelli. (05 Mar 2000) |
| cerebellar cyst | A cyst usually occurring in the lateral cerebellar white matter; often a part of cerebellar astrocytoma. (05 Mar 2000) |
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