Pattern of inborn errors of metabolism in an Omani population of the Arabian Peninsula

Annals of Tropical Paediatrics

Volumn 22, Issue 1, 2002, Pages 93-96

  Joshi, S N ^a   Hashim, J ^a   Venugopalan, P ^a  

^a SULTAN QABOOS UNIVERSITY HOSPITAL   (Oman)

Author keywords

[No Author keywords available]

Indexed keywords

METABOLISM;

ACIDURIA; ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL PROTOCOL; CONSANGUINITY; CONTROLLED STUDY; DIET THERAPY; DISEASE EXACERBATION; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; DISORDERS OF CARBOHYDRATE METABOLISM; FEMALE; FOLLOW UP; HUMAN; INBORN ERROR OF METABOLISM; INFANT; LACTIC ACIDOSIS; LYSOSOME STORAGE DISEASE; MAJOR CLINICAL STUDY; MALE; OMAN; SCREENING TEST; TANDEM MASS SPECTROMETRY; UREA CYCLE;

ADOLESCENT; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; FEMALE; FOLLOW-UP STUDIES; HUMANS; INFANT; INFANT, NEWBORN; LYSOSOMAL STORAGE DISEASES; MALE; METABOLISM, INBORN ERRORS; OMAN; RETROSPECTIVE STUDIES;

EID: 0036128631     PISSN: 02724936     EISSN: None     Source Type: Journal    
DOI: 10.1179/027249302125000238     Document Type: Article

References (10)

1. Incidence of inborn errors of metabolism in British Columbia, 1969-1996
2. Diagnosis of inborn errors of metabolism
3. Genetic disorders among Arab populations
4. Consanguinity in different regions of Saudi Arabia
5. Director-General of Planning
6. Diagnostic approach to inborn errors of metabolism in an emergency unit
7. Diagnosis of inborn errors of metabolism by tandem mass spectrometry
8. Automated tandem mass spectrometry for mass newborn screening for disorders in fatty acid, organic acid, and amino acid metabolism
9. A study of consanguinity in the Sultanate of Oman
10. Knowledge acquisition, management and representation for the diagnostic support in human inborn errors of metabolism