Hypokalaemia and paralysis in the Thai population

Nephrology Dialysis Transplantation

Volumn 19, Issue 8, 2004, Pages 2013-2018

  Phakdeekitcharoen, Bunyong ^a   Ruangraksa, Chatuporn ^a   Radinahamed, Piyanuch ^a  

^a MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Distal renal tubular acidosis (dRTA); Hypokalaemia; Hypokalaemic periodic paralysis (HypoPP); Periodic paralysis; Thyrotoxic periodic paralysis (TPP)

Indexed keywords

ADULT; ANAMNESIS; ARTICLE; BLOOD SAMPLING; CHEMICAL ANALYSIS; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENDER; GROUPS BY AGE; HUMAN; HYPERTHYROIDISM; HYPOKALEMIA; KIDNEY CALCIFICATION; LOADING TEST; MALE; METABOLIC ACIDOSIS; MUTATIONAL ANALYSIS; NEPHROLITHIASIS; ONSET AGE; PARALYSIS; POPULATION RESEARCH; PRIORITY JOURNAL; REGIONALIZATION; SEX RATIO; SYMPTOMATOLOGY; THAILAND; THYROID DISEASE; THYROID FUNCTION TEST; THYROTOXICOSIS; URINALYSIS;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; FEMALE; HUMANS; HYPOKALEMIC PERIODIC PARALYSIS; MALE; MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROSPECTIVE STUDIES; SEROEPIDEMIOLOGIC STUDIES; THAILAND;

EID: 4344646657     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/gfh328     Document Type: Article

References (19)

1. Ptacek LJ, Tawil R, Griggs RC et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994; 77: 863-868
2. Fontaine B, Vale Santos JM, Jurkat-Rott K et al. Mapping of hypokalemic periodic paralysis (HypoPP) to chromosome 1q31-q32 in three European families. Nature Genet 1994; 6: 267-272
3. Sillen A, Sorensen T, Kantola I, Friis ML, Gustavson HL, Wadelius KH. Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families. Am J Med Genet 1997; 69: 102-106
4. Jurkat-Rott K, Mitrovic N, Hang C et al. Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. Proc Natl Acad Sci, USA 2000; 97: 9549-9554
5. Bulman DE, Scoggan KA, Van Oene MD et al. A novel sodium channel mutation in a family with hypokalemic periodic paralysis. Neurology 1999; 53: 1932-1936
6. Abbott GW, Butler MH, Bendahhou S, Dalakas MC, Ptacek LJ, Goldstein AN. MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis. Cell 2001; 104: 217-231
7. Lin SH, Lin YF, Halperin ML. Hypokalemia and paralysis. Q J Med 2001; 94: 133-139
8. Satoyoshi E, Murakami K, Kowa H et al. Periodic paralysis in hyperthyroidism. Neurology 1963; 13: 746-752
9. McFadzean AJS, Yeung R. Periodic paralysis complicating thyrotoxicosis in Chinese. Br Med J 1967; 1: 451-455
10. Ko Ko GTC, Chow CC, Yeung VTF, Chan HHL, Li JKY, Cockram CS. Thyrotoxic periodic paralysis in a Chinese population. Q J Med 1996; 89: 463-468
11. Morris RC Jr, Ives HE. Inherited disorders of the renal tubule. In: Brenner BM, ed. Brenner and Rector's the Kidney, 5th edn. W.B. Saunders, Philadephia; 1991: 1764-1782
12. Sitprija V, Tungsanga K, Eiam-Ong S et al. Metabolic syndromes caused by decreased activity of ATPases. Semin Nephrol 1991; 11: 249-252
13. Wrong O, Davies H. The excretion of acid in renal disease. Q J Med 1959; 28: 259-313
14. Buckalew VM Jr, McCurdy DK, Ludwig GD, Chaykin LB, Elkinton JR. The syndrome of incomplete renal tubular acidosis. Am J Med 1968; 45: 32-42
15. Dias da Silva MR, Cerutti JM, Tengan CH et al. Mutations linked to familial hypokalaemic periodic paralysis in the calcium channel alpha1 subunit gene (Cav1.1) are not associated with thyrotoxic hypokalaemic periodic paralysis. Clin Endocrinol 2002; 56: 367-375
16. Shoffner JM. Molecular analysis of oxidative phosphorylation disease for detection of mitocondrial DNA mutation. In: Dracopoli NC, Haines JL, Korf BR et al., eds. Current Protocols in Human Genetics 9. John Wiley and Sons, London; 1998: 9.9.1-9.9.26
17. Fouad G, Dalakas M, Servidei S et al. Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis. Neuromuscul Disord 1997; 7: 33-38
18. Tanphaichitr VS, Sumboonnanonda A, Ideguchi H et al. Novel AE1 mutations in distal renal tubular acidosis: loss-of-function is rescued by glycophorin A. J Clin Invest 1998; 102: 2173-2179
19. Domrongkitchaiporn S, Pongsakul C, Stitchantrakul W et al. Bone mineral density and histology in distal renal tubular acidosis. Kidney Int 2001; 59: 1086-1093