Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP

Por um escritor misterioso
Last updated 21 janeiro 2025
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Rubinstein&#x2013;Taybi syndrome (RSTS) is a rare genetic disorder characterized by dysmorphic facial features, broad thumbs and halluces, intellectual disability, and postnatal growth retardation. This report presents a male infant with microcephaly and characteristic facial features, namely, low anterior hairline, hirsutism, thin upper lip and micrognathia, broad thumbs and first toes, cryptorchidism, recurrent pneumonia, developmental delay, and growth retardation. Genetic testing showed a novel pathogenic variant in the <i>CREBBP</i> gene which is consistent with the clinical diagnosis of RSTS.
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Rubinstein–Taybi syndrome: clinical and molecular overview
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
child with features of RSTS Download Scientific Diagram
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Rubinstein-Taybi Syndrome: Child Characteristics and Parental
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
PDF) Clinical exome sequencing identifies novel CREBBP variants in
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
A case with Rubinstein-Taybi syndrome: A novel frameshift mutation
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Full article: 8th Excellence in Pediatrics Conference - 2016 Book
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
PDF) Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Photographs of patient face, hands, and feet described with CREBBP
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
PDF) An unusual presentation of Rubinstein-Taybi Syndrome with
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Fourteen causative CREBBP mutations detected by direct sequencing
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Otopalatodigital Syndrome, Type I disease: Malacards - Research
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Rubinstein–Taybi syndrome: clinical and molecular overview
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Rubinstein–Taybi syndrome in diverse populations - Tekendo

© 2014-2025 progresstn.com. All rights reserved.