Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature.
Valentina TrevisanAnna MeroniChiara LeoniFabio SirchiaDavide PolitanoGiacomo FiandrinoValentina GiorgioDonato RiganteDomenico LimongelliLucrezia PerriElisabetta SforzaFrancesca LeonardiGermana ViscogliosiIlaria ContaldoDaniela OrteschiLuca ProiettiGiuseppe ZampinoRoberta OnesimoPublished in: Genes (2024)
The scattered information regarding the condition and the dearth of data on its natural history and developmental outcomes restrict genetic counseling, particularly in prenatal settings. Moreover, a prompt diagnosis is frequently delayed by the negative selection of trisomic cells in blood, with mosaicism percentage varying among tissues, which often entails the need for further testing. Purpose/topic: The aim of our work is to provide assistance in prenatal and postnatal genetic counseling by systematically delineating the current knowledge of the condition. This entails defining the prenatal and postnatal characteristics of the condition and presenting novel data from three cases, both prenatally and postnatally. Additionally, we report the developmental outcomes observed in two new patients.
Keyphrases
- pregnant women
- preterm infants
- electronic health record
- end stage renal disease
- ejection fraction
- induced apoptosis
- newly diagnosed
- healthcare
- genome wide
- big data
- smoking cessation
- prognostic factors
- type diabetes
- hiv testing
- patient reported outcomes
- adipose tissue
- health information
- oxidative stress
- data analysis
- deep learning
- hiv infected
- social media
- artificial intelligence
- antiretroviral therapy
- human immunodeficiency virus
- pi k akt