| Literature DB >> 33925963 |
Patrycja Juchniewicz1, Ewa Piotrowska2, Anna Kloska1, Magdalena Podlacha2, Jagoda Mantej2, Grzegorz Węgrzyn2, Stefan Tukaj2, Joanna Jakóbkiewicz-Banecka1.
Abstract
Through the use of new genomic and metabolomic technologies, our comprehension of the molecular and biochemical etiologies of genetic disorders is rapidly expanding, and so are insights into their varying phenotypes. Dosage compensation (lyonization) is an epigenetic mechanism that balances the expression of genes on heteromorphic sex chromosomes. Many studies in the literature have suggested a profound influence of this phenomenon on the manifestation of X-linked disorders in females. In this review, we summarize the clinical and genetic findings in female heterozygotic carriers of a pathogenic variant in one of ten selected X-linked genes whose defects result in metabolic disorders.Entities:
Keywords: X chromosome inactivation; X-linked inheritance; XCI; inborn errors of metabolism; metabolic disorders
Year: 2021 PMID: 33925963 DOI: 10.3390/ijms22094514
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923