Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Susceptibility to thyrotoxic periodic paralysis 1

Susceptibility to thyrotoxic periodic paralysis type 1 is defined by variations in the calcium channel gene CACNA1S.

Systematic

Hyperthyroidism
Familial gestational hyperthyroidism
Graves disease
McCune-Albright syndrom
Non-autoimmune hyperthyroidism
Susceptibility to thyrotoxic periodic paralysis 1
CACNA1S

References:

1.

Kung AW et al. (2004) Association of novel single nucleotide polymorphisms in the calcium channel alpha 1 subunit gene (Ca(v)1.1) and thyrotoxic periodic paralysis.

external link
2.

None (1985) Familial "hashitoxic' periodic paralysis.

external link
3.

Kusakabe T et al. (1976) Thyrotoxic periodic paralysis: a peculiar case with unusual dystonic behavior and variable relations of paralysis to serum potassium levels.

external link
4.

Au KS et al. (1972) Thyrotoxic periodic paralysis. Periodic variation in the muscle calcium pump activity.

external link
5.

Yeung RT et al. (1974) Thyrotoxic periodic paralysis. Effect of propranolol.

external link
6.

Layzer RB et al. (1974) Periodic paralysis caused by abuse of thyroid hormone.

external link
7.

Bernard JD et al. (1972) Thyrotoxic periodic paralysis in Californians of Mexican and Filipino ancestry.

external link
8.

McFadzean AJ et al. (1967) Periodic paralysis complicating thyrotoxicosis in Chinese.

external link
9.

Kilpatrick RE et al. (1994) Thyrotoxic hypokalemic periodic paralysis: report of four cases in black American males.

external link
10.

Sternberg D et al. (2003) Lack of association of the potassium channel-associated peptide MiRP2-R83H variant with periodic paralysis.

external link
11.

Jurkat-Rott K et al. (2004) Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation.

external link
12.

None (2006) Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge.

external link
13.

Shah N et al. (1979) Familial periodic paralysis and hyperthyroidism.

external link
14.

None (1975) Letter: fibre content of bread.

external link
15.

Dias Da Silva MR et al. (2002) A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis.

external link
16.

OMIM.ORG article

Omim 188580 external link
Update: Aug. 14, 2020
Copyright © 2005-2024 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD
Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944
Sitemap | Webmail | Disclaimer | Privacy Issues | Website Credits