Molekulargenetische Diagnostik
Praxis Dr. Mato Nagel

Neigung zur thyreotoxischen periodischen Paralyse 1

Die Neigung zu thyreotoxischer periodischer Paralyse Typ 1 wird bestimmt durch Variationen im CACNA1S-Gen.

Gliederung

Störungen des Schilddrüsenhormonsystems
Basedow-Krankheit
Neigung zur thyreotoxischen periodischen Paralyse 1
CACNA1S
Neonataler Diabetes mellitus mit angeborener Hypothyreose
Schilddrüsenhormonresistenz

Referenzen:

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.

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2.

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

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3.

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

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4.

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

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5.

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

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6.

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

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7.

None (1975) Letter: fibre content of bread.

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8.

None (1985) Familial "hashitoxic' periodic paralysis.

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9.

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

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10.

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

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11.

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

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12.

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

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13.

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

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14.

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

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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.

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