| familial osseous d. |
Morquio's syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| familial p. |
multiple adenomatous polyps with high malignant potential, lining the mucous membrane of the intestine, particularly the colon, beginning at about puberty. It occurs in several autosomal dominant conditions, including Gardner's syndrome, Peutz-Jeghers syndrome, and Turcot's syndrome. Called also p. coli., familial intestinal p., and multiple familial p.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial paroxysmal c. |
Mount-Reback syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial periodic f. |
a rare autosomal dominant syndrome that includes an abnormality on the cell receptor for tumor necrosis factor; characteristics include periodic fever with any of various skin disorders lasting for four days to three weeks, as well as mild systemic manifestations such as abdominal pain, headache, and chest pain. Called also tumor necrosis factor receptor–associated periodic syndrome.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| familial periodic p. |
an autosomal dominant condition marked by recurring attacks of rapidly progressive flaccid paralysis; there are three types: I, associated with a fall in serum potassium (hypokalemic periodic p.); II, associated with a rise in serum potassium (hyperkalemic periodic p.; called also Gamstorp's disease); and III, with normal potassium levels (normokalemic periodic p.).
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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