A novel NONO nonsense variant in a fetus with renal abnormalities.
Laia Rodriguez-RevengaAlfons NadalVirginia BorobioMaria Isabel Álvarez-MoraIrene MadrigalMontse PautaAntoni BorrellPublished in: Prenatal diagnosis (2023)
At 16 + 6-weeks a fetal scan performed in the second pregnancy of a 42 y.o. woman identified a right multicystic dysplastic kidney, left renal agenesis, absent urinary bladder, myocardial hypertrophy, increased nuchal fold, a single umbilical artery, and oligohydramnios. Trio exome sequencing analysis detected a novel pathogenic NONO variant. Postmortem examination after the termination of pregnancy confirmed the ultrasound findings and also revealed pulmonary hypoplasia, retrognathia and low-set ears. The variant was a novel de novo hemizygous pathogenic loss-of-function variant in NONO [NM_007363.5], associated with a rare X-linked recessive neurodevelopmental disorder, named intellectual developmental disorder, X-linked syndromic 34 (OMIM#300967). The postnatal characteristic features of this disorder include intellectual disability, developmental delay, macrocephaly, structural abnormalities involving the corpus callosum and/or cerebellum, left ventricular noncompaction and other congenital heart defects. In the prenatal setting, the phenotype has been poorly described, with all described cases presenting with heart defects. This case highlights the need of further clinical delineation to include renal abnormalities in the prenatal phenotype spectrum.
Keyphrases
- intellectual disability
- left ventricular
- autism spectrum disorder
- pregnant women
- heart failure
- preterm birth
- single cell
- magnetic resonance imaging
- computed tomography
- case report
- pregnancy outcomes
- acute myocardial infarction
- gene expression
- mitral valve
- magnetic resonance
- acute coronary syndrome
- percutaneous coronary intervention
- copy number
- coronary artery disease
- congenital heart disease
- aortic stenosis
- contrast enhanced ultrasound
- aortic valve