Press Kit

by | Oct 15, 2018

Press Kit Welcome to the CdLS Foundation’s online press kit. This section contains information for media working on stories about CdLS. CdLS Quick Facts CdLS is a genetic syndrome present from birth. There is no cure for CdLS. CdLS occurs in approximately 1 in...

Diagnosis of CdLS

by | Oct 15, 2018

Diagnosis of CdLS Currently, researchers find a gene change in about 75 percent of individuals with CdLS. A higher percentage may be identifiable as testing procedures become more sophisticated, and as additional genes are identified. What are the long-term...

Research Articles

by | Oct 11, 2018

Research Reviews The CdLS Foundation provides information on a range of research articles, most of which are accessible through PubMed, an online portal of research publications. Articles related to CdLS go back to the 1980s and are divided by topic. To access a...

Management Guidelines

by | Oct 10, 2018

Management Guidelines Treatment Guidelines for Preventive Care The treatment guideline sheet highlights routine care for individuals with CdLS at different ages, including infancy, early and late childhood, adolescence and adulthood. View Guidelines Developmental...

2005

by | Oct 4, 2018

CdLS Foundation Research Grants 2005 Awards A Mouse Model of Cornelia de Lange Syndrome Principal Investigator: Arthur Lander, MD, PhD, University of California, Irvine, CA. Award: $10,000 The methods of genetic engineering have allowed us to introduce mutations...