Galactosemia in three Filipino patients - The importance of newborn screening
Acta Medica Philippina
; : 15-17, 2009.
Article
in En
| WPRIM
| ID: wpr-633835
Responsible library:
WPRO
ABSTRACT
Disorders of galactose metabolism can be fatal if not treated early. Newborn screening has made it possible to detect and treat this disease. Three cases of galactosemia, one with galactokinase deficiency and two with galactose-1-phosphate uridyltransferase deficiency detected by newborn screening, are presented. Because of early detection and management, the first patient was spared the early complications of galactosemia and continues to grow and develop normally. The two other patients were diagnosed at 1 month, initial presentation included hepatomegaly and failure to thrive. Institution of treatment was able to reverse the acute complications and both are currently doing well. The importance of galactosemia newborn screening in preventing complications resulting from the disease is emphasized.
Full text:
1
Database:
WPRIM
Main subject:
Biological Phenomena
/
Neonatal Screening
/
Early Diagnosis
/
Failure to Thrive
/
Physiological Phenomena
/
Galactose
/
Galactosemias
/
Hepatomegaly
Type of study:
Diagnostic_studies
/
Screening_studies
Limits:
Humans
/
Infant
/
Male
Language:
En
Journal:
Acta Medica Philippina
Year:
2009
Document type:
Article