Rubinstein Taybi syndrome (RSTS) also known as Broad Thumb Hallux Syndrome characterized by distinct facial features with beaked or straight nose, short stature, moderate to severe intellectual disability, broad thumb and big toe. We report an interesting case of female child with history and examination suggestive of RSTS with Nephrotic syndrome. Investigation revealed presence of albumin in urine with hypercholesterolemia and hypoalbuminemia. Purpose of this case report is to highlight the distinctive presentation of this syndrome and to update the current state of knowledge
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
BACKGROUND Rubinstein-Taybi syndrome (RSTS) is a congenital disorder characterised by growth reta...
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 ge...
ObjectiveRubinstein-Taybi Syndrome is a rare genetic disorder with characteristic featuresincluding ...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RTS) is a congenital disorder characterized by typical facial features, b...
Objective Rubinstein-Taybi Syndrome is a rare genetic disorder with characteristic features includin...
Rubinstein-Taybi Syndrome (RSTS) is a rare genetic disorder. Individuals are characterized by broad ...
Congenital nephrotic syndrome (CNS) is a rare disorder characterized by massive proteinuria, hypoalb...
Rubinstein-Taybi syndrome (RSTS) is a rare, congenital, plurimalformative, and neurodevelopmental di...
Rubinstein-Taybi Syndrome (RTS) is a multiple congenital anomaly syndrome characterized by mental re...
Abstract Background Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant neurodevelopmental...
Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by faci...
Rubinstein-Taybi syndrome (RTS) is a rare multiple congenital anomalies-intellectual disability synd...
Congenital nephrotic syndrome is a rare inherited disorder arising from defects in the proteins of ...
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
BACKGROUND Rubinstein-Taybi syndrome (RSTS) is a congenital disorder characterised by growth reta...
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 ge...
ObjectiveRubinstein-Taybi Syndrome is a rare genetic disorder with characteristic featuresincluding ...
BackgroundRubinstein-Taybi syndrome (RSTS) is an extremely rare autosomal dominant genetic disease, ...
Rubinstein-Taybi syndrome (RTS) is a congenital disorder characterized by typical facial features, b...
Objective Rubinstein-Taybi Syndrome is a rare genetic disorder with characteristic features includin...
Rubinstein-Taybi Syndrome (RSTS) is a rare genetic disorder. Individuals are characterized by broad ...
Congenital nephrotic syndrome (CNS) is a rare disorder characterized by massive proteinuria, hypoalb...
Rubinstein-Taybi syndrome (RSTS) is a rare, congenital, plurimalformative, and neurodevelopmental di...
Rubinstein-Taybi Syndrome (RTS) is a multiple congenital anomaly syndrome characterized by mental re...
Abstract Background Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominant neurodevelopmental...
Rubinstein-Taybi syndrome or Broad Thumb-Hallux syndrome is a genetic disorder characterized by faci...
Rubinstein-Taybi syndrome (RTS) is a rare multiple congenital anomalies-intellectual disability synd...
Congenital nephrotic syndrome is a rare inherited disorder arising from defects in the proteins of ...
Rubinstein-Taybi syndrome (RSTS) is an autosomal dominant disorder, caused by loss-of-function varia...
BACKGROUND Rubinstein-Taybi syndrome (RSTS) is a congenital disorder characterised by growth reta...
A boy with classical Rubinstein-Taybi syndrome but no detectable mutation in the CREBBP and EP300 ge...