Matches in SemOpenAlex for { <https://semopenalex.org/work/W4200020975> ?p ?o ?g. }
- W4200020975 endingPage "474" @default.
- W4200020975 startingPage "465" @default.
- W4200020975 abstract "Skeletal disorders, including both isolated and syndromic brachydactyly type E, derive from genetic defects affecting the fine tuning of the network of pathways involved in skeletogenesis and growth-plate development. Alterations of different genes of this network may result in overlapping phenotypes, as exemplified by disorders due to the impairment of the parathyroid hormone/parathyroid hormone-related protein pathway, and obtaining a correct diagnosis is sometimes challenging without a genetic confirmation. Five patients with Albright's hereditary osteodystrophy (AHO)-like skeletal malformations without a clear clinical diagnosis were analyzed by whole-exome sequencing (WES) and novel potentially pathogenic variants in parathyroid hormone like hormone (PTHLH) (BDE with short stature [BDE2]) and TRPS1 (tricho-rhino-phalangeal syndrome [TRPS]) were discovered. The pathogenic impact of these variants was confirmed by in vitro functional studies. This study expands the spectrum of genetic defects associated with BDE2 and TRPS and demonstrates the pathogenicity of TRPS1 missense variants located outside both the nuclear localization signal and the GATA ((A/T)GATA(A/G)-binding zinc-containing domain) and Ikaros-like binding domains. Unfortunately, we could not find distinctive phenotypic features that might have led to an earlier clinical diagnosis, further highlighting the high degree of overlap among skeletal syndromes associated with brachydactyly and AHO-like features, and the need for a close interdisciplinary workout in these rare patients. © 2021 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR)." @default.
- W4200020975 created "2021-12-31" @default.
- W4200020975 creator A5005587302 @default.
- W4200020975 creator A5016435019 @default.
- W4200020975 creator A5017386401 @default.
- W4200020975 creator A5020934020 @default.
- W4200020975 creator A5026035922 @default.
- W4200020975 creator A5033940713 @default.
- W4200020975 creator A5039973207 @default.
- W4200020975 creator A5044615622 @default.
- W4200020975 creator A5049341852 @default.
- W4200020975 creator A5055283559 @default.
- W4200020975 creator A5055920819 @default.
- W4200020975 creator A5056903402 @default.
- W4200020975 creator A5059356998 @default.
- W4200020975 creator A5064594935 @default.
- W4200020975 creator A5065428803 @default.
- W4200020975 creator A5068739311 @default.
- W4200020975 creator A5070949543 @default.
- W4200020975 creator A5083390653 @default.
- W4200020975 date "2022-01-17" @default.
- W4200020975 modified "2023-09-26" @default.
- W4200020975 title "Novel Pathogenetic Variants in <scp><i>PTHLH</i></scp> and <scp><i>TRPS1</i></scp> Genes Causing Syndromic Brachydactyly" @default.
- W4200020975 cites W138352100 @default.
- W4200020975 cites W1569766571 @default.
- W4200020975 cites W187264608 @default.
- W4200020975 cites W1983448619 @default.
- W4200020975 cites W1992500414 @default.
- W4200020975 cites W1995499476 @default.
- W4200020975 cites W2006784180 @default.
- W4200020975 cites W2018856496 @default.
- W4200020975 cites W2034757205 @default.
- W4200020975 cites W2037458235 @default.
- W4200020975 cites W2045714596 @default.
- W4200020975 cites W2072788472 @default.
- W4200020975 cites W2074706861 @default.
- W4200020975 cites W2075308619 @default.
- W4200020975 cites W2080548729 @default.
- W4200020975 cites W2092501395 @default.
- W4200020975 cites W2117860124 @default.
- W4200020975 cites W2126202517 @default.
- W4200020975 cites W2145652037 @default.
- W4200020975 cites W2151296818 @default.
- W4200020975 cites W2193522503 @default.
- W4200020975 cites W2233975806 @default.
- W4200020975 cites W2325300404 @default.
- W4200020975 cites W2341713409 @default.
- W4200020975 cites W2342403040 @default.
- W4200020975 cites W2401368322 @default.
- W4200020975 cites W2471206328 @default.
- W4200020975 cites W2581793210 @default.
- W4200020975 cites W2588667445 @default.
- W4200020975 cites W2811181045 @default.
- W4200020975 cites W2885044037 @default.
- W4200020975 cites W2896597270 @default.
- W4200020975 cites W2915374540 @default.
- W4200020975 cites W2969926565 @default.
- W4200020975 cites W3109204401 @default.
- W4200020975 doi "https://doi.org/10.1002/jbmr.4490" @default.
- W4200020975 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34897794" @default.
- W4200020975 hasPublicationYear "2022" @default.
- W4200020975 type Work @default.
- W4200020975 citedByCount "3" @default.
- W4200020975 countsByYear W42000209752023 @default.
- W4200020975 crossrefType "journal-article" @default.
- W4200020975 hasAuthorship W4200020975A5005587302 @default.
- W4200020975 hasAuthorship W4200020975A5016435019 @default.
- W4200020975 hasAuthorship W4200020975A5017386401 @default.
- W4200020975 hasAuthorship W4200020975A5020934020 @default.
- W4200020975 hasAuthorship W4200020975A5026035922 @default.
- W4200020975 hasAuthorship W4200020975A5033940713 @default.
- W4200020975 hasAuthorship W4200020975A5039973207 @default.
- W4200020975 hasAuthorship W4200020975A5044615622 @default.
- W4200020975 hasAuthorship W4200020975A5049341852 @default.
- W4200020975 hasAuthorship W4200020975A5055283559 @default.
- W4200020975 hasAuthorship W4200020975A5055920819 @default.
- W4200020975 hasAuthorship W4200020975A5056903402 @default.
- W4200020975 hasAuthorship W4200020975A5059356998 @default.
- W4200020975 hasAuthorship W4200020975A5064594935 @default.
- W4200020975 hasAuthorship W4200020975A5065428803 @default.
- W4200020975 hasAuthorship W4200020975A5068739311 @default.
- W4200020975 hasAuthorship W4200020975A5070949543 @default.
- W4200020975 hasAuthorship W4200020975A5083390653 @default.
- W4200020975 hasBestOaLocation W42000209751 @default.
- W4200020975 hasConcept C104317684 @default.
- W4200020975 hasConcept C126322002 @default.
- W4200020975 hasConcept C127716648 @default.
- W4200020975 hasConcept C134018914 @default.
- W4200020975 hasConcept C16671776 @default.
- W4200020975 hasConcept C2777871287 @default.
- W4200020975 hasConcept C2781133459 @default.
- W4200020975 hasConcept C2781208988 @default.
- W4200020975 hasConcept C519063684 @default.
- W4200020975 hasConcept C54355233 @default.
- W4200020975 hasConcept C60644358 @default.
- W4200020975 hasConcept C64618202 @default.
- W4200020975 hasConcept C71924100 @default.
- W4200020975 hasConcept C75563809 @default.