PMID: 25229967Sep 18, 2014Paper

DiGeorge syndrome in a neonate

Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Kai-Ju LuoWen Li

Abstract

No abstract listed.

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22q11 Deletion Syndrome

22q11.2 deletion syndrome, also known as DiGeorge syndrome, is a congenital disorder caused by a partial deletion of chromosome 22. Symptoms include heart defects, poor immune system function, a cleft palate, complications related to low levels of calcium in the blood, and delayed development. Discover the latest research on this disease here.

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