Differences in DNA methylation status explain phenotypic variability in patients with 5p− syndrome

Differences in DNA methylation status explain phenotypic variability in patients with 5p− syndrome

Abstract Cri Du Chat syndrome, or 5p− syndrome, is characterized by a terminal or interstitial deletion on the short arm of chromosome 5 that causes variable clinical manifestations, including high-pitched cry in newborns, delayed growth, and global development. Different cytogenomic rearrangements,...

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Bibliographic Details
Main Authors: Vanessa Tavares Almeida, Samar N. Chehimi, Gleyson F. S. Carvalho, Yanca Gasparini, Amom M. Nascimento, Lucas L. Vieira, Beatriz M. Wolff, Marília M. Montenegro, Leslie D. Kulikowski
Format: Article
Language:English
Published: BMC 2024-04-01
Series:BMC Research Notes
Subjects:
Cri du chat syndrome
DNA methylation
Rare diseases
Online Access:https://doi.org/10.1186/s13104-024-06734-7

Internet

https://doi.org/10.1186/s13104-024-06734-7

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