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Article

[Dravet syndrome diagnostics].

Ugeskrift for laeger - 22 Feb 2010

Hansen Lars Kjaersgård, Rasmussen Niels Henrik, Ousager Lilian Bomme

Abstract excerpt

Dravet syndrome is an epileptic syndrome of infancy. We describe the features of two cases with genetically verified SCNA1 mutations. The diagnosis was established rather late in one case. The epilepsies were medically intractable and the symptoms characteristic of Dravet syndrome. The children r...

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PMID: 20184820

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20184820-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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