PEHO syndrome is a progressive encephalopathy with edema, hypsarrhythmia and optic atrophy. It is a very rare disease, one of the Finnish heritage diseases, and has ...
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for PEHO syndrome
Summary. PEHO (Progressive encephalopathy with Edema, Hypsarrhythmia and Optic atrophy) syndrome is a rare neurodegenerative disorder belonging to the group of ...
Background. PEHO syndrome is a rare neurodegenerative condition which usually begins within the first few weeks of life. The condition takes its name from the ...
Summarizes the current understanding of Progressive Encephalopathy with edema, Hypsarrhythmia, and Optic atrophy (PEHO syndrome).
1. Brain Dev. 2001 Nov;23(7):765-9. The PEHO syndrome. Riikonen R(1). Author information: (1)Department of Child Neurology, University Hospital, P.O ...
The progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome is a pediatric disorder of unknown origin, characterized by a combi
PEHO syndrome. Synonym: Infantile cerebello-optic atrophy. Inheritance: Thought to be autosomal recessive. A rare neurodegenerative syndrome first reportes on 1991.
PEHO syndrome symptoms, causes, diagnosis, and treatment information for PEHO syndrome (Encephalopathy progressive - optic atrophy) with alternative diagnoses, full ...
Progressive encephalopathy with edema, hypsarrhythmia, and optic nerve atrophy (PEHO) syndrome is a rare, apparently autosomal recessive condition in which ...