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. 2019 Sep 13;10:988. doi: 10.3389/fneur.2019.00988

Table 4.

Phenotypic spectrum of patients with KCNQ2, SCN2A, or PRRT2 pathogenic variants.

PRRT2 (n = 10) KCNQ2 (n = 5) SCN2A (n = 4)
Epilepsy syndrome
Benign familial infantile (n = 5) Benign familial neonatal (n = 2) Ohtahara syndrome (n = 1)
Unclassified (n = 3)
Benign infantile (n = 3) Ohtahara syndrome (n = 1)
Unclassified
(n = 2)
Unclassified
(n = 2)
Drug responsiveness
   Self-limited 8 3 1
   Drug responsive 2 1 1
   Drug resistant 1 2
Developmental disability
   Normal 8 3 0
Intellectual disability 1 2 3
   ADHD*/ASD* 1 0 1
*

ADHD, attention deficit hyperactivity disorder; ASD, autism spectrum disorder.