Absence of collagen flowers on electron microscopy and identification of (likely) pathogenic COL5A1 variants in two patients
Two probands are reported with pathogenic and likely pathogenic COL5A1 variants (frameshift and splice site) in whom no collagen flowers have been identified with transmission electron microscopy (TEM). One proband fulfils the clinical criteria for classical Ehlers-Danlos syndrome (cEDS) while the o...
Những tác giả chính: | Angwin, C, Brady, A, Colombi, M, Ferguson, D, Pollitt, R, Pope, F, Ritelli, M, Symoens, S, Ghali, N, Van Dijk, F |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
MDPI
2019
|
Những quyển sách tương tự
-
Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
Bằng: Chloe Angwin, et al.
Được phát hành: (2023-04-01) -
Identification of the novel COL5A1 c.3369_3431dup, p.(Glu1124_Gly1144dup) variant in a patient with incomplete classical Ehlers–Danlos syndrome: The importance of phenotype‐guided genetic testing
Bằng: Marco Ritelli, et al.
Được phát hành: (2020-10-01) -
Transcriptome analysis of skin fibroblasts with dominant negative COL3A1 mutations provides molecular insights into the etiopathology of vascular Ehlers-Danlos syndrome.
Bằng: Nicola Chiarelli, et al.
Được phát hành: (2018-01-01) -
Clinical and molecular characterization of an 18‐month‐old infant with autosomal recessive cutis laxa type 1C due to a novel LTBP4 pathogenic variant, and literature review
Bằng: Marco Ritelli, et al.
Được phát hành: (2019-07-01) -
Case report and discussion: Pre-implantation genetic diagnosis with surrogacy in vascular Ehlers–Danlos syndrome
Bằng: Chloe Angwin, et al.
Được phát hành: (2023-03-01)