Progressive Pseudorheumatoid Dysplasia resolved by whole exome sequencing: a novel mutation in WISP3 and review of the literature
Abstract Background Progressive pseudorheumatoid dysplasia (PPRD) is a rare autosomal-recessive, non-inflammatory arthropathy, shown to be caused by mutations in the WNT1-inducible signaling pathway protein 3 (WISP3) gene. Although several hundred cases were reported worldwide, the diagnosis remains...
Saved in:
Main Authors: | Ben Pode-Shakked (Author), Asaf Vivante (Author), Ortal Barel (Author), Shai Padeh (Author), Dina Marek-Yagel (Author), Alvit Veber (Author), Shachar Abudi (Author), Aviva Eliyahu (Author), Irit Tirosh (Author), Shiri Shpilman (Author), Shirlee Shril (Author), Friedhelm Hildebrandt (Author), Mordechai Shohat (Author), Yair Anikster (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2019-03-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Refining the Phenotypic Spectrum of KMT5B-Associated Developmental Delay
by: Aviva Eliyahu, et al.
Published: (2022) -
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies
by: Irit Tirosh, et al.
Published: (2019) -
Delayed-onset of progressive pseudorheumatoid dysplasia in a Chinese adult with a novel compound WISP3 mutation: a case report
by: Qiongyi Hu, et al.
Published: (2017) -
Coexistence of a novel WISP3 pathogenic variant and an MEFV mutation in an Arabic family with progressive pseudorheumatoid dysplasia mimicking polyarticular juvenile idiopathic arthritis
by: Basil M. Fathalla, et al.
Published: (2020) -
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom
by: Shani Karklinsky, et al.
Published: (2022)