These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: The ironies of human mind: a case of Rett syndrome. Author: Chattopadhyay S, Arora R. Journal: Ethiop J Health Sci; 2014 Apr; 24(2):171-4. PubMed ID: 24795519. Abstract: BACKGROUND: Rett Syndrome (RS) is a chromosome X-linked genetic neurological disorder characterized by developmental regression, particularly in relation to expressive language and use of the hands. It is also associated with profound mental retardation and almost exclusively affects females. CASE DETAILS: A four and a half year old girl reported to our dental OPD for a dental checkup. On complete examination, she was diagnosed to be suffering from Rett syndrome. Preventive therapies and proper oral hygiene instructions were explained to her mother. CONCLUSION: Early diagnosis of such disorders is extremely important along with treatment of patients' problems with love and care to prevent them from further pain and stress.[Abstract] [Full Text] [Related] [New Search]