| Literature DB >> 33291480 |
Susan M Motch Perrine1, Meng Wu2, Greg Holmes2, Bryan C Bjork3, Ethylin Wang Jabs2, Joan T Richtsmeier1.
Abstract
The phenotype currently accepted as Pierre Robin syndrome/sequence/anomalad/complex (PR) is characterized by mandibular dysmorphology, glossoptosis, respiratory obstruction, and in some cases, cleft palate. A causative sequence of developmental events is hypothesized for PR, but few clear causal relationships between discovered genetic variants, dysregulated gene expression, precise cellular processes, pathogenesis, and PR-associated anomalies are documented. This review presents the current understanding of PR phenotypes, the proposed pathogenetic processes underlying them, select genes associated with PR, and available animal models that could be used to better understand the genetic basis and phenotypic variation of PR.Entities:
Keywords: Treacher Collins; cleft palate; mandible; micrognathia; nasopharynx; stickler; tongue; velocardiofacial syndrome
Year: 2020 PMID: 33291480 PMCID: PMC7768358 DOI: 10.3390/jdb8040030
Source DB: PubMed Journal: J Dev Biol ISSN: 2221-3759