Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations

• Published in: European journal of medical genetics Vol. 63; no. 1; p. 103624
• Main Authors: Monteiro, Fabiola P., Curry, Cynthia J., Hevner, Robert, Elliott, Stephen, Fisher, Jamie H., Turocy, John, Dobyns, William B., Costa, Larissa A., Freitas, Erika, Kitajima, João Paulo, Kok, Fernando
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Masson SAS 01.01.2020
• Subjects: Arthrogryposis; ATP1A2; Fetal akinesia sequence; Malformations of cortical development; Na+/K+- ATPase; ATP1A2; Fetal akinesia sequence; Arthrogryposis; Na+/K+- ATPase; Malformations of cortical development; Na(+)/K(+)- ATPase
• ISSN: 1769-7212; 1878-0849; 1878-0849
• DOI: 10.1016/j.ejmg.2019.01.014

The Na+/K+- ATPase acts as an ion pump maintaining the essential plasma membrane potential in all mammalian cell types, and is essential for many cellular functions. There are four α isoforms (α1, α2, α3 and α4) with distinct expression patterns, kinetic properties and substrate affinity. The α2-isoform is encoded by ATP1A2 and evidence supports its utmost importance in Cl− homeostasis in neurons, and in the function of respiratory neurons at birth. Monallelic pathogenic variants in ATP1A2 are associated with familial hemiplegic migraine type 2 (FHM2) and on rare occasions with alternating hemiplegia of childhood 1 (AHC1). To date, no instances of biallelic loss of function variants have been reported in humans. However, Atp1a2 homozygous loss of function knockout mice (α2−/− mice) show severe motor deficits, with lack of spontaneous movements, and are perinatally lethal due to absent respiratory activity. In this report we describe three newborns from two unrelated families, who died neonatally, presenting in utero with an unusual form of fetal hydrops, seizures and polyhydramnios. At birth they had multiple joint contractures (e.g. arthrogryposis), microcephaly, malformations of cortical development, dysmorphic features and severe respiratory insufficiency. Biallelic loss of function variants in ATP1A2, predicted to be pathogenic were found on whole exome sequencing. We propose that this is a distinctive new syndrome caused by complete absence of Na+/K+- ATPase α2-isoform expression.