Heterotopic Ossification in a Neonate with DiGeorge Syndrome.

Indian Journal of Pediatrics
Rajeev GuptaMala Kumar

Abstract

No abstract listed.

References

Nov 1, 2012·Malaysian Orthopaedic Journal·Ss KhooA Jeffry
Feb 9, 2021·Journal of Pediatric Genetics·Bruna Lixinski DinizPaulo Ricardo Gazzola Zen

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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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