Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
Por um escritor misterioso
Last updated 24 dezembro 2024
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.
Rubinstein-Taybi Syndrome: A Complete Overview — DermNet
Photographs of patient face, hands, and feet described with CREBBP
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PDF) Epigenetic Mechanisms of Rubinstein–Taybi Syndrome
Genes, Free Full-Text
child with features of RSTS Download Scientific Diagram
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