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

Por um escritor misterioso

Descrição

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
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
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Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
PDF) Lacrimal drainage anomalies in Rubinstein-Taybi syndrome
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
PDF) Rubinstein-Taybi syndrome medical guidelines
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
A novel CREBBP mutation and its phenotype in a case of Rubinstein
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP
genetic test report depicting disease and inheritance
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