The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures
Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751).
Gespeichert in:
| Autor*in: |
van Roest, Aalt [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2020 |
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| Schlagwörter: |
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| Umfang: |
6 |
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| Übergeordnetes Werk: |
Enthalten in: Biologically active vallesamine, strychnan, and rhazinilam alkaloids from - Lim, Jun-Lee ELSEVIER, 2015, ejpn : official journal of the European Paediatric Neurology Society, Burlington, Mass |
|---|---|
| Übergeordnetes Werk: |
volume:24 ; year:2020 ; pages:148-153 ; extent:6 |
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| DOI / URN: |
10.1016/j.ejpn.2019.12.003 |
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The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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Self-limited (familial) infantile epilepsy (S(F)IE), formerly known as benign (familial) infantile convulsions (B(F)IC), is an infantile cluster epilepsy with in rule a complete recovery. This form of epilepsy is most often caused by variations in the PRRT2 gene (OMIM #605751). |
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The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures |
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