Phenotypic continuum between POLE-related recessive disorders: A case report and literature review.

Abstract

POLE is a pleiotropic gene with phenotypic expression of pathogenic variants depending on the type of variant, impact on the protein, and mode of inheritance. Heterozygous missense variants located within the exonuclease domain have been shown to result in polymerase proofreading-associated polyposis (PPAP) which is characterized by an increased risk for colon polyps and colorectal cancer. Biallelic variants resulting in markedly reduced amounts of normal protein have been reported in two separate recessive pediatric syndromes: facial dysmorphism, immunodeficiency, livedo, and short stature as well as intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenital, and genital anomalies. Here we report two siblings identified to have POLE c.1686 + 32C > G in trans with POLE p.(Glu709*) via exome sequencing. A detailed review of the reported phenotypes in these two siblings and from available literature revealed that individuals with biallelic POLE pathogenic variants resulting in partial loss-of-function present with a similar phenotype: short stature and facial dysmorphism with or without immunodeficiency. These data suggest a phenotypic continuum between the previously reported POLE-related recessive disorders.

• Authors: Maegan E Roberts, Sarah Nimrichter, Megan L Marshall, Elizabeth K Flynn, Rick Person, Kathleen S Hruska, Paul Kruszka, Jane Juusola
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 188 Issue 10 Pg. 3121-3125 (10 2022) ISSN: 1552-4833 [Electronic] United States
• PMID: 35860951 (Publication Type: Case Reports, Review)
• Copyright: © 2022 Wiley Periodicals LLC.

Topics

• Dwarfism (diagnosis, genetics)
• Humans
• Musculoskeletal Abnormalities
• Mutation, Missense
• Osteochondrodysplasias (genetics)
• Phenotype
• Exome Sequencing