Clinical characteristics on manifestation and gene mutation of a transient neonatal cyanosis: A case report.

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ID: 90075
2020
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Abstract
We analyzed the main features of an infant diagnosed with temporary neonatal cyanosis in order to strengthen our understanding of the disease.We report a patient diagnosed with temporary neonatal cyanosis. The main clinical characteristics, gene mutation and treatment are discussed and a review of related literature was conducted. The neonate aged 1 d and 5 h was admitted to hospital due to cyanosis after birth. The main clinical manifestation was cyanosis, which was not improved by auxiliary ventilation and the patient showed no obvious shortness of breath or methemoglobinemia. Gene mutation analysis showed a heterozygous c.190C>T mutation in the gene associated with transient neonatal cyanosis, which was derived from his mother. Symptomatic supportive treatment was given for 2 mo. The neonate was discharged and gradually improved with oral administration of vitamin C and vitamin B2 for 2 wk.There is no special treatment for temporary neonatal cyanosis caused by heterozygous mutation of the gene.
Reference Key
yuan2020clinicalworld Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Yuan, Jing;Zhu, Xue-Ping;
Journal World journal of clinical cases
Year 2020
DOI
10.12998/wjcc.v8.i1.217
URL
Keywords
case report cyanosis genetic mutation hbg2 methemoglobinemia temporary neonatal cyanosis

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