Web Directory

» Cranial Magnetic Resonance Imaging Mistakenly Suggests Prenatal Ischaemia in PEHO-Like Syndrome
   Longman, Tolmie, McWilliam and MacLennan describe two sisters with a PEHO-like syndrome, for the eldest of whom cranial magnetic resonance imaging revealed periventricular white matter changes, whilst cerebellar hypoplasia, characteristic of true PEHO syn
   http://www.ncbi.nlm.nih.gov/pubmed/12868478

» Infantile Cerebello-Optic Atrophy
   Haltia and Somer describe eight cases of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (PEHO syndrome).
   http://www.ncbi.nlm.nih.gov/pubmed/8460530

» Online Mendelian Inheritance in Man
   Summarizes the current understanding of Progressive Encephalopathy with edema, Hypsarrhythmia, and Optic atrophy (PEHO syndrome).
   http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=260565

» PEHO syndrome
   Somer describes a number of Finnish cases.
   http://www.ncbi.nlm.nih.gov/pubmed/8301648

» Progressive Encephalopathy with Edema, Hypsarrhythmia, and Optic Atrophy (PEHO syndrome) in Two Japanese Siblings
   Fujimoto et al report on two Japanese siblings with PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy), the first case report of PEHO syndrome outside Finland.
   http://www.ncbi.nlm.nih.gov/pubmed/8552220