Seckel syndrome

	WikiDoc Resources for Seckel syndrome
Articles
Most recent articles on Seckel syndrome Most cited articles on Seckel syndrome Review articles on Seckel syndrome Articles on Seckel syndrome in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Seckel syndrome Images of Seckel syndrome Photos of Seckel syndrome Podcasts & MP3s on Seckel syndrome Videos on Seckel syndrome
Evidence Based Medicine
Cochrane Collaboration on Seckel syndrome Bandolier on Seckel syndrome TRIP on Seckel syndrome
Clinical Trials
Ongoing Trials on Seckel syndrome at Clinical Trials.gov Trial results on Seckel syndrome Clinical Trials on Seckel syndrome at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Seckel syndrome NICE Guidance on Seckel syndrome NHS PRODIGY Guidance FDA on Seckel syndrome CDC on Seckel syndrome
Books
Books on Seckel syndrome
News
Seckel syndrome in the news Be alerted to news on Seckel syndrome News trends on Seckel syndrome
Commentary
Blogs on Seckel syndrome
Definitions
Definitions of Seckel syndrome
Patient Resources / Community
Patient resources on Seckel syndrome Discussion groups on Seckel syndrome Patient Handouts on Seckel syndrome Directions to Hospitals Treating Seckel syndrome Risk calculators and risk factors for Seckel syndrome
Healthcare Provider Resources
Symptoms of Seckel syndrome Causes & Risk Factors for Seckel syndrome Diagnostic studies for Seckel syndrome Treatment of Seckel syndrome
Continuing Medical Education (CME)
CME Programs on Seckel syndrome
International
Seckel syndrome en Espanol Seckel syndrome en Francais
Business
Seckel syndrome in the Marketplace Patents on Seckel syndrome
Experimental / Informatics
List of terms related to Seckel syndrome

	Seckel syndrome;
ICD-10	Q87.1
OMIM	210600
DiseasesDB	31625

Overview

The Seckel syndrome or microcephalic primordial dwarfism is a congenital nanosomic disorder supposed to be caused by defects of genes on chromosome 3 and 18. One form of Seckel syndrome can be caused by mutation in the gene encoding ataxia-telangiectasia and RAD3-related protein (ATR) which maps to chromosome 3q22.1-q24. This gene is central in the cell's DNA damage response and repair mechanism.