Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)

Pediatric Neurology

Volumn 15, Issue 4, 1996, Pages 337-339

  Shevell, Michael I ^a   Colangelo, Patricia ^a   Treacy, Eileen ^a   Polomeno, Robert C ^a   Rosenblatt, B ^a  

^a MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ANTICONVULSIVE AGENT; CLONAZEPAM; LAMOTRIGINE; PHENYTOIN; PREDNISONE; VALPROIC ACID; VIGABATRIN;

ARTICLE; BRAIN DISEASE; CASE REPORT; CEREBELLUM ATROPHY; CHILD; CLINICAL FEATURE; EDEMA; FEMALE; HUMAN; HYPSARRHYTHMIA; INTRACTABLE EPILEPSY; OPTIC NERVE ATROPHY; PRIORITY JOURNAL; SYNDROME;

ATROPHY; BRAIN EDEMA; CEREBELLUM; CHILD, PRESCHOOL; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; NEUROLOGIC EXAMINATION; OPTIC ATROPHY; SPASMS, INFANTILE; SYNDROME;

EID: 0030297609     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(96)00161-0     Document Type: Article

References (8)

1. [1] Salonen R, Somer M, Haltia M, Lorentz M. Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO syndrome). Clin Genet 1991;39:287-93.
2. [2] Somer M, Sainio K. Epilepsy and the electroencephalogram in progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). Epilepsia 1993;34:727-31.
3. [3] Somer M, Salonen O, Pihko H, Norio R. PEHO syndrome (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy): Neuroradiologic findings. AJNR 1993;14:861-7.
4. [4] Haltia M, Somer M. Infantile cerebello-optic atrophy; Neuropathology of the progressive encephalopathy syndrome with edema, hypsarrhythmia and optic atrophy (the PEHO syndrome). Acta Neuropathol 1993;85:241-7.
5. [5] Somer, M. Diagnositc criteria and genetics of the PEHO syndrome. J Med Genet 1993;30:932-6.
6. [6] Fujimoto S, Yokochi K, Nakano M, Wada Y. Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome) in two Japanese siblings. Neuropediatrics 1995;26:270-2.
7. [7] De Braekeleer M. Les genes déletères. In: Bouchard G, De Braekeleer M, eds. Histoire d'un génome. Sillery: Presses de l'Université du Québec, 1991:345-64.
8. [8] Jensen PR, Hansen FJ, Skovby F. Cerebellar hypoplasia in children with the carbohydrate-deficient glycoprotein syndrome. Neuroradiology 1995;37:328-30.