[PEHO syndrome (progressive encephalopathy, edema, hypsarrhythmia. optic atrophy)]

Autor:	K, Hollódy, K, Kollár
Rok vydání:	1997
Předmět:	Male Fetal Growth Retardation Infant Newborn Electroencephalography Syndrome Magnetic Resonance Imaging Optic Atrophy Pregnancy Seizures Child Preschool Edema Humans Abnormalities Multiple Brain Damage Chronic Female Spasms Infantile
Zdroj:	Orvosi hetilap. 138(7)
ISSN:	0030-6002
Popis:	The authors report the case of a now 2-year-old boy with PEHO syndrome. The syndrome is rare and it has not been published yet in Hungary. The syndrome was named after the first letters of its main characteristic signs: progressive encephalopathy, edema, hypsarrhythmia and optic atrophy. The aetiology of the syndrome is still unknown. Autosomal recessive inheritance is likely. The prognosis is poor. Intractable infantile spasms and the arrest of the psychomotoric and mental development can be expected.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid________::99fc88b8b7afc73d0dd1f06d1be3856e https://pubmed.ncbi.nlm.nih.gov/9091844 Zobrazit plný text záznamu