Neonatal presentation of COG6‐CDG with prominent skin phenotype
Abstract Many of the genetic childhood disorders leading to death in the perinatal period follow autosomal recessive inheritance and bear specific challenges for genetic counseling and prenatal diagnostics. Often, affected children die before a genetic diagnosis can be established, thereby precludin...
Main Authors: | Katalin Komlosi, Selina Gläser, Julia Kopp, Alrun Hotz, Svenja Alter, Andreas D. Zimmer, Carmela Beger, Stefan Heinzel, Christoph Schmidt, Judith Fischer |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2020-09-01
|
Series: | JIMD Reports |
Subjects: | |
Online Access: | https://doi.org/10.1002/jmd2.12154 |
Similar Items
-
Case Report: DPM1-CDG: Novel Variant with Severe Phenotype and Literature Review
by: Hanna Lausmann, et al.
Published: (2022-07-01) -
Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran
by: Atefe Papi, et al.
Published: (2023-02-01) -
The Swedish COG6‐CDG experience and a comprehensive literature review
by: Zhi‐Jie Xia, et al.
Published: (2023-01-01) -
Restrictive dermopathy: Report of two cases
by: Anisha K Janardhanan, et al.
Published: (2018-01-01) -
PMM2‐CDG caused by uniparental disomy: Case report and literature review
by: Laurien Vaes, et al.
Published: (2020-07-01)