Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
Descrição
Rubinstein-Taybi syndrome is an intellectual disability which causes short stature, distinctive facial features, and varying cognitive deficits.
Rubinstein-Taybi Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Rubinstein-Taybi syndrome: MedlinePlus Genetics
Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations - Van‐Gils - 2019 - Clinical Genetics - Wiley Online Library
Rubinstein–Taybi Syndrome in a Filipino Infant with a Novel CREBBP Gene Pathogenic Variant
Rubinstein-Taybi Syndrome 1
BJORL - Brazilian Journal of Otorhinolaryngology
Identification of 22q11.2 deletion in a patient with schizophrenia and clinically diagnosed Rubinstein–Taybi syndrome - Nagai - 2022 - Psychiatry and Clinical Neurosciences Reports - Wiley Online Library
Rubinstein-Taybi Syndrome - an overview
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Rubinstein-Taybi Syndrome: Symptoms, Causes, Treatment
Rubinstein-Taybi syndrome: Treatments and life expectancy
A case of Rubinstein-Taybi Syndrome with a CREB-binding protein gene mutation
Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management, Italian Journal of Pediatrics
Clinical photos of the patients. (a) Case 1: Dysmorphic facial features
DBMCI MDS : Formerly MDS Experts - RUBINSTEIN TAYBI SYNDROME An autosomal dominant disease associated with deletions of the short arm of ch 16. Clinical Features: - Mental retardation - Broad thumbs
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