| PD | Doctor of Pharmacy; Dublin Pharmacopoeia; interpupillary distance; Paget disease; pancreatic duct; p... |
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| GOH | geroderma osteodysplastica hereditaria |
| KHM | keratoderma hereditaria mutilans |
| LH | late healing; lateral hypothalamic [syndrome]; left hand; left heart; left hemisphere; left hyperpho... |
| THH | telangiectasia hereditaria haemorrhagica; trichohyalin |
| PCT | Porphyria Cutanea Tarda |
|---|---|
| PD | Pars distalis |
| PPD | proximal pars distalis |
| RPD | rostal pars distalis |
| porphyria cutanea tarda hereditaria | A form of hepatic porphyria (porphyria, hepatic) characterised by photosensitivity resulting in bullae that rupture easily to form shallow ulcers. This condition occurs in two forms: a sporadic, nonfamilial form that begins in middle age and has normal amounts of uroporphyrinogen decarboxylase with diminished activity in the liver; and a familial form in which there is an autosomal dominant inherited deficiency of uroporphyrinogen decarboxylase in the liver and red blood cells. (12 Dec 1998) |
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| syphilis hereditaria tarda | Syphilis, believed to be congenital, but not manifesting itself until several years after birth. (05 Mar 2000) |
| myopathia | <medicine> Any affection of the muscles or muscular system. Origin: NL, fr. Gr, a muscle +, to suffer. Source: Websters Dictionary (01 Mar 1998) |
| adynamia episodica hereditaria | Hyperkalaemic periodic paralysis, without myotonia. (05 Mar 2000) |
| articulatio radioulnaris distalis | The pivot synovial joint between the head of the ulna and the ulnar notch on the radius; an articular disk passes across the distal part of the joint. Synonym: articulatio radioulnaris distalis, distal radioulnar articulation, inferior radioulnar joint. (05 Mar 2000) |
| pars distalis | The larger part of the adenohypophysis composed of cords of epithelial cells individually specialised to secrete various tropic hormones that exert their effect on several target organs in the body. The secretory activity of these cells is under the control of either releasing or inhibiting factors elaborated by hypothalamic neurons and transported to the adenohypophysis by the hypothalamo-hypophysial portal system. Synonym: pars distalis. (05 Mar 2000) |
| protocoproporphyria hereditaria | Porphyria characterised by abdominal pain and neuropsychiatric abnormalities, by dermal sensitivity to light and mechanical trauma, by increased faecal excretion of proto-and coproporphyrin, and by increased urinary excretion of d-aminolevulinic acid, porphobilinogen, and porphyrins; due to a deficiency of protoporphyrinogen oxidase; autosomal dominant inheritance. Synonym: protocoproporphyria hereditaria, South African type porphyria. (05 Mar 2000) |
| syphilis hereditaria | <radiology> Wimberger sign, periostitis, part of ToRCHS complex (12 Dec 1998) |
| distalis | <anatomy> Remote, farther from any point of reference, opposed to proximal. <dentistry> Used to designate a position on the dental arch farther from the median line of the jaw. Origin: L. Distans = distant (18 Nov 1997) |
| tuberositas phalangis distalis | A roughened raised surface of horseshoe shape on the palmar surface of the distal end of the terminal or ungual phalanx of each finger and toe, which serves to support the pulp of the digit. Synonym: tuberositas phalangis distalis, tuberositas unguicularis, ungual tuberosity. (05 Mar 2000) |
| facies distalis dentis | The contact surface of a tooth that is directed away from the median plane of the dental arch; opposite to the mesial surface of a tooth. Synonym: facies distalis dentis. (05 Mar 2000) |
| rachitis tarda | <pathology> A condition marked by softening of the bones (due to impaired mineralisation, with excess accumulation of osteoid), with pain, tenderness, muscular weakness, anorexia and loss of weight, resulting from deficiency of vitamin D and calcium. Origin: Gr. Malakia = softness (18 Nov 1997) |
| porphyria cutanea tarda | A form of hepatic porphyria (porphyria, hepatic) characterised by photosensitivity resulting in bullae that rupture easily to form shallow ulcers. This condition occurs in two forms: a sporadic, nonfamilial form that begins in middle age and has normal amounts of uroporphyrinogen decarboxylase with diminished activity in the liver; and a familial form in which there is an autosomal dominant inherited deficiency of uroporphyrinogen decarboxylase in the liver and red blood cells. (12 Dec 1998) |
| porphyria cutanea tarda symptomatica | A form of hepatic porphyria (porphyria, hepatic) characterised by photosensitivity resulting in bullae that rupture easily to form shallow ulcers. This condition occurs in two forms: a sporadic, nonfamilial form that begins in middle age and has normal amounts of uroporphyrinogen decarboxylase with diminished activity in the liver; and a familial form in which there is an autosomal dominant inherited deficiency of uroporphyrinogen decarboxylase in the liver and red blood cells. (12 Dec 1998) |
| neurosis tarda | Neurotic patterns developing in older people, related to organic cerebral lesions. (05 Mar 2000) |
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