Acinar Dysplasia in a Full-Term Newborn with a NKX2.1 Variant

Abstract

Acinar dysplasia (AcDys) is one of the three main diffuse developmental disorders of the lung. The transcription factor NK2 homeobox 1 (NKX2.1) partly controls the synthesis of surfactant proteins by type 2 alveolar epithelial cells (AEC2), and germline mutations are known to be associated with brain-lung thyroid syndrome. We report the case of a full-term neonate who developed refractory respiratory failure with pulmonary hypertension requiring venoarterial extracorporeal membrane oxygenation. Histological examination of the lung biopsy specimen was consistent with the diagnosis of AcDys. Molecular analyses led to the identification of the missense heterozygous variant in <i>NKX2.1</i> (NM_001079668) c.731A&gt;G p.(Tyr244Cys), which is predicted to be pathogenic. After 5 weeks, because AcDys is a fatal disorder and the patient’s status worsened, life-sustaining therapies were withdrawn, and she died after a few hours. This study is the first to extend the phenotype of <i>NKX2.1</i> pathogenic variant, to a fatal form of AcDys.