Epidemiological and Clinical Study of Phenylketonuria (PKU) Disease in the National Screening Program of Neonates, Fars Province, Southern Iran
Background: Classic phenylketonuria (PKU) is a rare metabolic disorder that results from a deficiency of a liver enzyme known as phenylalanine hydroxylase (PAH). In this study, we researched about PKU epidemiological factors and health quality of patients after the neonatal screening program. Method...
Saved in:
Main Authors: | S Senemar (Author), H Ganjekarimi (Author), M Fathzadeh (Author), B Tarami (Author), M Bazrgar (Author) |
---|---|
Format: | Book |
Published: |
Tehran University of Medical Sciences,
2009-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Epidemiological and Clinical Study of Phenylketonuria (PKU) Disease in the National Screening Program of Neonates, Fars Province, Southern Iran
by: S Senemar, et al.
Published: (2009) -
The Prevalence and Clinical Study of Galactosemia Disease in a Pilot Screening Program of Neonates, Southern Iran
by: B Tarami, et al.
Published: (2011) -
The Prevalence and Clinical Study of Galactosemia Disease in a Pilot Screening Program of Neonates, Southern Iran
by: S Senemar, et al.
Published: (2011) -
Epidemiology and clinical study of phenylketonuria (PKU) patients in Khorasan Province; Norteast Iran
by: Negar Morovatdar, et al.
Published: (2015) -
Epidemiology and clinical study of phenylketonuria (PKU) patients in Khorasan Province; Norteast Iran
by: Negar Morovatdar, et al.
Published: (2015)