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Clinical genetics · 2025

Comprehensive Clinical and Genetic Characterization of a Spanish Cohort of 22 Patients With Bainbridge-Ropers Syndrome.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Trujillano Laura, Valenzuela Irene, Costa-Roger Mar, Cuscó Ivon, Fernandez-Alvarez Paula, Cueto-González Anna, Lasa-Aranzasti Amaia, Masotto Bárbara, Abulí Anna, Codina-Solà Marta, Del Campo Miguel, Ruiz Moreno Juan Antonio, Pardo Domínguez Cristina, Palma Milla Carmen, Pérez de la Fuente Rubén, Quesada-Espinosa Juan Francisco, Núñez-Enamorado Noemí, Gener Blanca, Ballesta-Martínez María Juliana, Brea-Fernández Alejandro J, Fernández-Prieto Montse, Trujillo-Quintero Juan Pablo, Ruiz Anna, Santos-Simarro Fernando, Rosello Mónica, Orellana Carmen, Martinez Francisco, Martinez-Monseny Antonio F, Casas-Alba Dídac, Serrano Mercedes, Palomares-Bralo María, Rikeros-Orozco Emi, Gómez-Cano María Ángeles, Tirado-Requero Pilar, Pié Juste Juan, Ramos Feliciano J, García-Arumí Elena, Tizzano Eduardo F

Аннотация

Bainbridge-Ropers Syndrome (BRPS) is a genetic condition resulting from truncating variants in the ASXL3 gene. The clinical features include neurodevelopmental and language impairments, behavioral issues, hypotonia, feeding difficulties, and distinctive facial features. In this retrospective study, we analyzed 22 Spanish individuals with BRPS, aiming to perform a detailed clinical and molecular description and establish a genotype-phenotype correlation. We identified 19 ASXL3 variants, nine of which are novel. We documented recurrence in nontwin siblings due to parental mosaicism. The predominant prenatal finding was intrauterine growth restriction (35%) followed, after birth, by feeding difficulties (90.5%), hypotonia (85.7%), and gastroesophageal reflux disease (82.4%). Later in life, intellectual disability, language impairment, autism spectrum disorder (75%), and joint laxity (73.7%) were noted. Individuals with variants in the 3' mutational cluster region (MCR) of exon 12 exhibited more perinatal feeding problems, and those with variants in the 5' MCR of exon 11 displayed lower percentiles in height and occipitofrontal circumference, as well as higher frequency of arched eyebrows. This study is the first characterization of a Spanish BRPS cohort, with more than 50 clinical features analyzed, representing the most detailed phenotypic analysis to date.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты