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Purpura fulminans in a newborn infant with galactosemia

✍ Scribed by Aysegul Zenciroglu; Mehmet Sah Ipek; Mustafa Aydin; Abdurrahman Kara; Nurullah Okumus; Mustafa Kilic

Book ID
106121954
Publisher
Springer
Year
2009
Tongue
English
Weight
193 KB
Volume
169
Category
Article
ISSN
0340-6997

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The spectrum of mutations in the Galactose-1-phosphate uridyl transferase (GALT) gene is described in 11 cases of classic galactosemia and 38 of Duarte-2 type identified by the Texas Newborn Screening Program. Blinded studies were done by automated DNA sequencing of all the 11 exons and the exon-int

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## Abstract Purpura fulminans (PF) is a severe disorder of acute onset with high morbidity and mortality. In children, this rapidly progressive illness is usually associated with severe bacterial or viral infections. However, some other conditions may participate in the development of PF. Our objec