# Transient Neonatal Cyanosis Exacerbated by Inhaled Nitric Oxide

**Authors:** Kaquanta Barlow, Charles J. Sadle, Vidhi Jhaveri, Nicole Cacho, Timothy E. Albertson, Payam Vali, Joseph J. Shen, Satyan Lakshminrusimha

PMC · DOI: 10.1055/a-2821-3305 · AJP Reports · 2026-03-17

## TL;DR

A newborn with cyanosis and low oxygen saturation was found to have methemoglobinemia, a hereditary condition, which was worsened by inhaled nitric oxide.

## Contribution

The paper highlights the importance of considering hereditary methemoglobinemia in newborns with unexplained cyanosis and elevated PaO2.

## Key findings

- Methemoglobin levels were elevated (10.2%) after discontinuation of inhaled nitric oxide.
- A heterozygous likely pathogenic variant in HBG2 (p.His63Tyr) was identified in the infant.
- Avoiding triggers like inhaled nitric oxide is crucial in managing hereditary methemoglobinemia.

## Abstract

Methemoglobinemia in newborns presents with cyanosis and hypoxemia, which can be mistaken for congenital heart disease or pulmonary hypertension.

A term infant presented with cyanosis and low SpO
2
(70s) immediately after birth, despite continuous positive airway pressure (CPAP) and 100% inspired oxygen. The patient was intubated and started on inhaled nitric oxide (iNO) and prostaglandin E1 infusion. Chest X-ray showed bilateral pneumothoraces; the echocardiogram was normal. Arterial blood gases demonstrated normal pH and elevated PaO
2
. iNO and prostaglandin E1 (PGE1) were discontinued. Attempts to obtain methemoglobin levels via a co-oximeter panel were unsuccessful, presumably due to out-of-range values. The infant's father revealed that he also had transient cyanosis as an infant. The infant was treated with ascorbic acid. A blood sample sent to a reference laboratory a day after discontinuation of inhaled NO showed a methemoglobin level of 10.2%. Targeted gamma globin gene sequencing found a heterozygous likely pathogenic variant in hemoglobin subunit gamma 2 (HBG2) (p.His63Tyr). He was discharged home at 1 week of age on room air.

Hereditary causes of methemoglobinemia should be considered for newborns with persistent cyanosis with low SpO
2
and elevated PaO
2
. Detailed family history and avoiding triggers of methemoglobinemia, such as iNO, are the cornerstones of management.

## Linked entities

- **Genes:** HBG2 (hemoglobin subunit gamma 2) [NCBI Gene 3048]
- **Diseases:** methemoglobinemia (MONDO:0001117), congenital heart disease (MONDO:0005453), pulmonary hypertension (MONDO:0005149)

## Full-text entities

- **Genes:** HBG2 (hemoglobin subunit gamma 2) [NCBI Gene 3048] {aka HBG-T1, TNCY}, HBG1 (hemoglobin subunit gamma 1) [NCBI Gene 3047] {aka HBG-T2, HBGA, HBGR, HSGGL1, PRO2979}
- **Diseases:** Methemoglobinemia (MESH:D008708), cyanosis (MESH:D003490), hypoxemia (MESH:D000860), congenital heart disease (MESH:D006330), Neonatal Cyanosis (OMIM:613977), pulmonary hypertension (MESH:D006976)
- **Chemicals:** NO (MESH:D009614), ascorbic acid (MESH:D001205), oxygen (MESH:D010100), SpO (-), Nitric Oxide (MESH:D009569), PGE1 (MESH:D000527)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.His63Tyr

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12995450/full.md

## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12995450/full.md

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Source: https://tomesphere.com/paper/PMC12995450