Episodic Pain Syndrome, Familial, 3
A rare, autosomal dominant disorder caused by mutation in the SCN11A gene. It is characterized by intense episodic pain mainly affecting the distal lower extremities in early childhood. The pain diminishes with age.
C125390
C3809899
Disease or Syndrome
Episodic Pain Syndrome, Familial, 3
Episodic Pain Syndrome, Familial, 3
FEPS3
Syndrome
Rare Non-Neoplastic Disorder