Full Text (PDF)
Case Report

A Rare Case of Rubinstein-Taybi Syndrome with Amelogenesis Imperfecta

Vishwajeet D. , Vishwajeet D. , Sujatha G. P. , Ashok L. , Kulkarnid

Author Information

Licence:




Indian Journal of Forensic Odontology 7(1-2):p 13-19, January - June 2014. | DOI:

How Cite This Article:


Timeline

Received : N/A         Accepted : N/A          Published : N/A

Abstract

Rubinstein-Taybi syndrome (RTS) is a rare congenital disorder characterized by typical facial features, broad thumbs and toes, with mental retardation. Additionally, tumors, keloids and various congenital anomalies including congenital heart defects have been reported in RTS patients. Here, we report a case of 11year-old female with a Rubinstein-Taybi syndrome associated with amelogenesis imperfecta having normal mental status with no cardiac abnormality.

Keywords: Rubinstein-Taybi Syndrome; Amelogenesis Imperfecta; Congenital Anomalies; Broad Thumbs and Toes.


References

No records found.


About this article


Cite this article


Licence:




Received Accepted Published
N/A N/A N/A

DOI:

Keywords


Article Level Metrics

Last Updated

Saturday 17 October 2026, 12:58:48 (IST)


1940

Accesses

4
267
00

Citations


NA
NA
NA

Download citation


Article Keywords


Keyword Highlighting

Highlight selected keywords in the article text.


Timeline


Received N/A
Accepted N/A
Published N/A

licence



Access this article



Share