Patrón-Romero Leslie, Lepe Marco Antonio Hernández, Torres José de Jesús Manríquez, Aguirre-Gómez Diego Daniel, Hayashi-Mercado Natsuo, Uribe Genaro Rodríguez, Cerón Tadeo, Ruiz-Gamboa María, Gándara-Mireles Jesús Alonso, Lares-Asseff Ismael, Loera-Castañeda Verónica, Alvelais-Palacios Jorge, Arzamendi-Cepeda Lucrecia, Castañeda-González Lidia Magdalena, García-Barrón Adolfo, Herrera Francisco Yamal Quiroz, González-Salazar Francisco, Almanza-Reyes Horacio
Faculty of Medicine and Psychology, Autonomous University of Baja California, Tijuana, Mexico.
University College London Hospital NHS Trust, London, UK.
Am J Med Genet A. 2025 Nov;197(11):e64181. doi: 10.1002/ajmg.a.64181. Epub 2025 Jul 9.
Keratosis-ichthyosis-deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American patient. Our aim is to establish extensive genotype-phenotype correlations, particularly in relation to the causes of death. Molecular studies enable us to confirm the disease's etiology and establish the causes of death with certain pathogenic variants. This information provides healthcare professionals with valuable guidelines for management and allows for the development of appropriate therapeutic strategies.
角化病-鱼鳞病-耳聋(KID)综合征是一种罕见的常染色体显性外胚层疾病,由GJB2基因突变引起,该基因编码位于13号染色体q12.11上的缝隙连接蛋白连接蛋白26(Cx26)。本研究首次呈现了与KID综合征相关的死亡率分析,重点是一位拉丁美洲患者的病例报告。我们的目标是建立广泛的基因型-表型相关性,特别是与死亡原因相关的相关性。分子研究使我们能够确认该疾病的病因,并确定某些致病变异的死亡原因。这些信息为医疗保健专业人员提供了宝贵的管理指南,并有助于制定适当的治疗策略。