Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Por um escritor misterioso
Descrição
Rubinstein–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.
Full article: 8th Excellence in Pediatrics Conference - 2016 Book
Otopalatodigital Syndrome, Type I disease: Malacards - Research
EP300‐related Rubinstein–Taybi syndrome: Highlighted rare
PDF) Case Report: Rubinstein-Taybi Syndrome
Photographs of patient face, hands, and feet described with CREBBP
Exon deletions of the EP300 and CREBBP genes in two children with
Pediatric on Squares on X: Rubinstein Taybi Syndrome #Pediatric
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Frontiers Case report: A preterm infant with rubinstein-taybi
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP
de
por adulto (o preço varia de acordo com o tamanho do grupo)