# Germline mosaicism in TCF20-associated neurodevelopmental disorders: a case study and literature review

## TL;DR

This paper reports a case of germline mosaicism in a TCF20-related neurodevelopmental disorder, highlighting its potential role in inherited conditions.

## Contribution

The study confirms germline mosaicism in TCF20 using ddPCR, offering physical evidence for a rare inheritance pattern.

## Key findings

- A novel TCF20 variant caused neurodevelopmental symptoms in two siblings.
- Germline mosaicism was confirmed via ddPCR in the father's urothelial cells.
- Germline mosaicism may be under-detected in neurodevelopmental disorders.

## Abstract

Autosomal dominant variants in transcription factor 20 (TCF20) can result in TCF20-associated neurodevelopmental disorder (TAND), a condition characterized by developmental delay and intellectual disability, autism, dysmorphisms, dystonia, and variable other neurological features. To date, a total of 91 individuals with TAND have been reported; ~67% of cases arose de novo, while ~10% were inherited, and, intriguingly, ~8% were either confirmed or suspected to have arisen via germline mosaicism. Here, we describe two siblings with a developmental condition characterized by intellectual disability, autism, a circadian rhythm sleep disorder, and attention deficit hyperactivity disorder (ADHD) caused by a novel heterozygous single nucleotide deletion in the TCF20 gene, NM_001378418.1:c.4737del; NP_001365347.1:p.Lys1579Asnfs*36 (GRCh38/hg38). The variant was not detected in DNA extracted from peripheral blood in either parent by Sanger sequencing of PCR-generated amplicons, or by deep sequencing of PCR amplicons using MiSeq and MinION. However, droplet digital PCR (ddPCR) of DNA derived from early morning urine detected the variation in 3.2% of the father’s urothelial cells, confirming germline mosaicism. This report is only the second to confirm with physical evidence TCF20 germline mosaicism and discusses germline mosaicism as a likely under-detected mode of inheritance in neurodevelopmental conditions.