Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Por um escritor misterioso
Last updated 23 fevereiro 2025
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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.
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Rubinstein–Taybi syndrome: clinical and molecular overview
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child with features of RSTS Download Scientific Diagram
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Rubinstein-Taybi Syndrome: Child Characteristics and Parental
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PDF) Clinical exome sequencing identifies novel CREBBP variants in
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A case with Rubinstein-Taybi syndrome: A novel frameshift mutation
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A novel CREBBP mutation and its phenotype in a case of Rubinstein
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Full article: 8th Excellence in Pediatrics Conference - 2016 Book
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PDF) Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
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Photographs of patient face, hands, and feet described with CREBBP
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PDF) An unusual presentation of Rubinstein-Taybi Syndrome with
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Fourteen causative CREBBP mutations detected by direct sequencing
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Otopalatodigital Syndrome, Type I disease: Malacards - Research
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Rubinstein–Taybi syndrome: clinical and molecular overview
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Rubinstein–Taybi syndrome in diverse populations - Tekendo
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