Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2011;11(1):20-8.

Recognition and diagnostic approach to acute metabolic disorders in the neonatal period

Affiliations
Review

Recognition and diagnostic approach to acute metabolic disorders in the neonatal period

Sarar Mohamed. Sudan J Paediatr. 2011.

Abstract

Inborn errors of metabolism (IEM) constitute a group of inherited disorders that cause significant neonatal morbidity and mortality. This diverse group of diseases present with different clinical manifestations that make the diagnosis a real challenge. Early detection and appropriate investigations prevent complications and save lives. The aim of this review is to enable general paediatricians to clinically recognize IEM and plan relevant investigations at the appropriate time in a cost-effective manner, especially in countries where resources are limited.

Keywords: Diagnosis; Inborn errors; Metabolism; Neonate.

PubMed Disclaimer

References

    1. Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW et al. (eds). The Metabolic and Molecular Bases of Inherited Disease. 8th ed New York; McGraw-Hill; 2001.
    1. Clarke JTR. A clinical guide to inherited metabolic diseases. 2nd ed Cambridge; University Press; 2002.
    1. Moammar H, Cheriyan G, Mathew R, Al-Sannaa N. Incidence and patterns of inborn errors of metabolism in the Eastern Province of Saudi Arabia, 1983-2008. Ann Saudi Med. 2010; 30(4): 271–7. - PMC - PubMed
    1. El-Said MF, BadiiR BMS, Shahbek N, El-Ali MG, El-Marikhie M, El-Zyoid M, et al. A common mutation in the CBS gene explains a high incidenceof homocystinuria in the Qatari population. Hum Mutat 2006; 27: 719–724. - PubMed
    1. Rashed MS, Rahbeeni Z, Ozand PT. Application of electrospray tandem mass spectrometry to neonatal screening. Semin Perinatal 1999; 23(2): 183–193 - PubMed

LinkOut - more resources