Reply to <i>Before scoliosis can be attributed to the variant c.326G>A in MYH3, its pathogenicity must be proven</i>
Dear Editor, We appreciate the valuable comments regarding our recent case report on a 15-year-old girl presenting with scoliosis, growth retardation, facial dysmorphism, and delayed puberty, who was found to carry the heterozygous NM_002470.4(MYH3):c.326G>A (p.Arg109His) variant.1 We welcome th...
Saved in:
Main Authors: | Maria Chiara Maccarone, Matilde Paramento, Edoardo Passarotto, Paola Contessa, Maria Rubega, Emanuela Formaggio, Stefano Masiero |
---|---|
Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2025-06-01
|
Series: | European Journal of Translational Myology |
Subjects: | |
Online Access: | https://www.pagepressjournals.org/bam/article/view/14034 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Before scoliosis can be attributed to the variant c.326G>A in MYH3, its pathogenicity must be proven
by: Josef Finsterer
Published: (2025-06-01) -
Clinical case of distal arthrogryposis in combination with epilepsy due to an unbalanced translocation
by: T. V. Kozhanova, et al.
Published: (2022-07-01) -
Identification of a de novo MYH9 mutation in a Chinese family with MYH9-related disease
by: Ruimin Cai, et al.
Published: (2025-12-01) -
Clinical and genetic characteristics of type 7 distal arthrogryposis caused by a pathogenic variant in the <i>MYH8</i> gene
by: I. V. Sharkova, et al.
Published: (2023-10-01) -
EEG Microstate as a Marker of Adolescent Idiopathic Scoliosis
by: M. Rubega, et al.
Published: (2024-01-01)