CdLS Online Family Album

Add your child to the Family Album or update your current listing

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Lily b. 2007 Oklahoma	Vanessa b. 2006 Florida	Kennedi b. 2005 Kentucky	Delaney b. 1999 Washington	Kayla b. 2003 New Mexico
Tyler b. 2000 Colorado	Daniel b. 1982 Washington	Mike b. 1971 New York	Nick b. 2001 New York	Scott b. 1989 California
Jack b. 2007 Texas	Kevin b. 1963 Arkansas	Kathryn b. 2007 Tennessee	Hayden b. 2000 California	Fletcher b. 2006 Maryland
Benjamin b. 2006 Maine	Michelle b. 1964 Oregon	Tayvion b. 2006 New York	Karli b. 1992 Utah	Ayzic b. 2004 Ohio
Gabe b. 2001 North Carolina	Lisa b. 1967 Pennsylvania	Ryan b. 1985 Connecticut	Payson b. 2001 Idaho	Julie b. 1967 Arizona

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The Cornelia de Lange Syndrome Foundation does not recommend or endorse any one product, method, resource, or service. All information contained here within is for the personal interest or investigation of the reader. Individuals included in this album may or may not have a confirmed diagnosis of CdLS. Information on treatment, medication, diet, etc., is not intended as a guide for self-treatment. Questions and concerns about treatment should be discussed with your doctor or other appropriate professionals.

Last Updated 1/21/08