A Case of Tyrosinemia Type III with Status Epilepticus and Mental Retardation

A Case of Tyrosinemia Type III with Status Epilepticus and Mental Retardation

Tyrosinemia type III is an autosomal recessive disorder caused by the deficiency of 4- hydroxyphenylpyruvate dioxygenase (4-HPPD). It is characterized by elevated levels of blood tyrosine and massive excretion of its derivatives into the urine. Clinical findings of tyrosinemia type III include neuro...

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Bibliographic Details
Main Authors: Reza Najafi, Neda Mostofizadeh, Mahin Hashemipour
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Advanced Biomedical Research
Subjects:
Mental retardation
status epilepticus
tyrosinemia type III
Online Access:http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=7;epage=7;aulast=Najafi

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http://www.advbiores.net/article.asp?issn=2277-9175;year=2018;volume=7;issue=1;spage=7;epage=7;aulast=Najafi

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