Andersen's syndrome: A distinct periodic paralysis

Annals of Neurology

Volumn 42, Issue 3, 1997, Pages 305-312

  Sansone, V ^a,c   Griggs, R C ^a   Meola, G ^b   Ptacek L J ^b   Barohn, R ^a   Lannaccone, S ^c   Bryan, W ^d   Baker, N ^e   Janas, S J ^d   Scott, W ^f   Ririe, D ^e   Tawil, R ^g  

^a UNIVERSITY OF MILAN   (Italy)

^b STRONG MEMORIAL HOSPITAL   (United States)

^c UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^e Pediatric Neurology   (United States)

^f TEXAS SCOTTISH RITE HOSPITAL FOR CHILDREN   (United States)

^g OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL; SODIUM CHANNEL;

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CLINICAL PROTOCOL; DISEASE ASSOCIATION; FACE DYSMORPHIA; FEMALE; GENETIC LINKAGE; GLYCOGEN STORAGE DISEASE TYPE 4; HEART VENTRICLE ARRHYTHMIA; HUMAN; HUMAN TISSUE; HYPERKALEMIA; HYPOKALEMIA; LONG QT SYNDROME; MALE; PERIODIC PARALYSIS; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CHILD; FEMALE; HUMANS; HYPOKALEMIA; MALE; PARALYSES, FAMILIAL PERIODIC; PEDIGREE; POINT MUTATION;

EID: 0030768672     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420306     Document Type: Article

References (33)

1. Klein R, Ganelin R, Marks JF, et al. Periodic paralysis with cardiac arrhythmia. J Pediatr 1963;62:371-385
2. Lehmann-Horn F, Engel A, Ricker K, Rudel R. The periodic paralyses and paramyotonia congenita. In: Engel AG, FranziniArmstrong C, eds. Myology. 2nd ed. New York: McGraw-Hill, 1994;1303-1334
3. Griggs RC. Periodic paralysis. Semin Neurol 1983;3:285-293
4. Lisak RP, LeBeau J, Tucker SH, Rowland LP. Hyperkalemic periodic paralysis with cardiac arrhythmia. Neurology 1970;20: 386 (Abstract)
5. Andersen ED, KrasilnikofF PA, Overvad H. Intermittent muscular weakness, extrasystoles, and multiple developmental abnormalities: a new syndrome? Acta Pediatr Scand 1971;60:559-564
6. Levitt LP, Rose LI, Dawson D. Hypokalemic periodic paralysis with arrhythmia. N Engl J Med 1972;286:253-254
7. Stubbs WA. Bidirectional ventricular tachycardia in familial hypokalemic periodic paralysis. Proc R Soc Med [Biol] 1976;69:223-224
8. Kramer LD, Cole JP, Messenger JC, Ellestad MH. Cardiac dysfunction in a patient with familial hypokalemic periodic paralysis. Chest 1979;75:189-192
9. Yoshimura T, Kaneuji M, Okuno T, et al. Periodic paralysis with cardiac arrhythmia. Eur J Pediatr 1983;140:338-343
10. Gould RJ, Steeg CN, Eastwood AB, et al. Potentially fatal cardiac dysrhythmia and hyperkalemic periodic paralysis. Neurology 1985;35:1208-1212
11. Fukuda K, Ogawa S, Yokozuka H, et al. Long-standing bidirectional tachycardia in a patient with hypokalemic periodic paralysis. J Electrocardiol 1988;21:71-76
12. Baquero JL, Ayala RA, Wang J, et al. Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation? Ann Neurol 1995;37:408-411
13. Tawil R, Ptacek LJ, Pavlakis SG, et al. Andersen's syndrome: potassium sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. Ann Neurol 1994;35:326-330
14. Ptacek LJ, Tyler F, Trimmer JS, et al. Analysis of a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus. Am J Hum Genet 1991;49:278-282
15. Ptacek LJ, George AL Jr, Griggs RC, et al. Identification of a mutation in the gene causing hyperkalemic periodic paralysis. Cell 1991;67:1021-1027
16. Fontaine B, Khurana TS, Hoffman EP, et al. Hyperkalemic periodic paralysis and the adult sodium channel ot-subunit gene. Science 1990;250:1000-1002
17. Keating M, Atkinson D, Dunn C, et al. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science 1991;252:704-706
18. Wang Q, Curran ME, Splawski I, et al. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996;12:17-23
19. Ptacek LJ, Tawil R, Griggs RC, et al. Dihydropyridine receptor mutations cause hypokalemic periodic paralysis. Cell 1994;77:863-868
20. McManis PG, Lambert EH, Daube JR. The exercise test in periodic paralysis. Muscle Nerve 1986;9:704-710
21. Schwanz PJ, Moss AJ, Vincent GM, Crampton RS. Diagnostic criteria for the long QT syndrome: an update. Circulation 1993;88:782-784
22. Martin AB, Perry JC, Robinson JL, et al. Calculation of QTc duration and variability in the presence of sinus arrhythmia. Am J Cardiol 1995;75:950-952
23. Rowland LP. Andersen's syndrome? Or Klein-Lisak-Andersen syndrome? Ann Neurol 1994;35:252-253 (Letter)
24. Rowland LP, Lisak RP. Periodic paralysis: K levels during arrhythmia. N Engl J Med 1972;287:50 (Letter)
25. Layzer RB, Lovelace RE, Rowland LP. Hyperkalemic periodic paralysis. Arch Neurol 1967;16:455-472
26. Lewis ED, Griggs RC, Moxley RT. Regulation of plasma potassium in hyperkalemic periodic paralysis. Neurology 1979;29:1131-1137
27. Marks ML, Trippel DL, Keating M. Long QT syndrome associated with syndactyly identified in females. Am J Cardiol 1995;76:744-745
28. Marks ML, Whisler SL, Clericuzio C, Keating' M. A new form of long QT syndrome associated with syndactyly. J Am Coll Cardiol 1995;25:59-64
29. Sperelakis N. Regulation of calcium slow channels of heart by cyclic nucleotides and effects of ischemia. Adv Pharmacol 1994;31:1-24
30. Rudel R, Ruppersberg JP, Spittelmeister W. Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica. Muscle Nerve 1989;12:281-287
31. Lehmann-Horn F, laizzo PA, Franke C, et al. Schwartz-Jampel syndrome: II. Na+ channel defect causes myotonia. Muscle Nerve 1990;13:528-535
32. Basson CT, Cowley GS, Solomon SD, et al. The clinical and genetic spectrum of the Holt-Oram syndrome (heart-hand syndrome). N Engl J Med 1994;330:885-891
33. Basson CT, Solomon SD, Weissman B, et al. Genetic heterogeneity of heart-hand syndromes. Circulation 1995;91:1326-1329