Identification of a de novoc.1000dela ank1 mutation associated to hereditary spherocytosis in a neonate with coombs-negative hemolytic jaundice-case reports

HIGHLIGHTS

• who: Lichun Xie from the (UNIVERSITY) have published the article: Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports, in the Journal: (JOURNAL)
• future: The case supports the position that a more rigorous approach is needed to find underlying causes of "idiopathic" severe neonatal jaundice.

SUMMARY

In 2,000 in people of Northern European descent. The clinical manifestations of HS in the neonatal age are typically hyperbilirubinemia followed by anemia. Owing to the commonness of neonatal jaundice, the . . .

 



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