Total: 2 |
|
PMID (PMCID) | ||
---|---|---|
15968934 |
MALE | Infant, Newborn |
Progressive encephalopathy with edema, hypsarrhythmia, and optic nerve atrophy (PEHO)-like syndrome: what diagnostic characteristics are defining? | ||
D'Arrigo S, Grazia BM, Faravelli F, Riva D, Pantaleoni C. J Child Neurol. 2005;20(5):454-6. |
||
We present the case of a child with PEHO-like syndrome and underline the need for a careful follow-up of these patients to identify signs and symptoms that can have a later onset, such as optic atrophy. | ||
12949965 |
MIXED_SAMPLE | Infant |
PEHO and PEHO-like syndromes: report of five Australian cases. | ||
Field MJ, Grattan-Smith P, Piper SM, Thompson EM, Haan EA, Edwards M, James S, Wilkinson I, Ades LC. Am J Med Genet A. 2003;122A(1):6-12. |
||
A PEHO-like syndrome has been described, in which the affected individuals have neither optic atrophy nor the typical neuroradiological findings. |