Title of article
Selective screening of 650 high risk Iranian patients for detection of inborn error of metabolism
Author/Authors
-، - نويسنده Neonatalogy Research center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Pishva, Narges , -، - نويسنده Neonatlaogy Research center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Mirzaee, Alie , -، - نويسنده Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Karamizade, Zohre , -، - نويسنده Neonatalogy Research center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Pourarian, Shahnaz , -، - نويسنده Neonatalogy Research center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Hemmati, Fariba , -، - نويسنده Neonatalogy Research center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences ,Shiraz, Iran Razvi, Mostajab , -، - نويسنده Neonatalogy Research Center, Department of Pediatrics, Namazee Hospital, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran Saki, Forough
Issue Information
فصلنامه با شماره پیاپی 0 سال 2015
Pages
4
From page
11
To page
14
Abstract
-
Abstract
Objective: Although metabolic diseases individually are rare ,but overall have an incidence of 1/2000 and can cause devastating and irreversible effect if not diagnosed early and treated promptly. selective screening is an acceptable method for detection of these multi presentation diseases.Method: using panel neonatal screening for detection of metabolic diseases in 650 high risk Iranian patients in Fars province. The following clinical features were used as inclusion criteria for investigation of the patients.Lethargy, poor feeding ,persistent vomiting, cholestasis, intractable seizure ,decreased level of consciousness ,persistent hypoglycemia, unexplained acid base disturbance and unexplained neonatal death.Result: Organic acidemia with 40 cases (42%) was the most frequent disorder diagnosed in our high risk populations, followed by disorder of galactose metabolism(30%), 15 patient had classic galactosemia(GALT
Journal title
Iranian Journal of Neonatology (IJN)
Serial Year
2015
Journal title
Iranian Journal of Neonatology (IJN)
Record number
2014080
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