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- Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
- Fragile X 101 (National Fragile X Foundation)Fragile X Syndrome/Symptoms ... Fragile X Syndrome ... There are many ways individuals and professionals learn about Fragile X. No matter how you got here, we are ...
- Marfan syndrome is a genetic disorder that causes problems with the development of connective tissue, which supports the body's bones, muscles, organs, & ...
- Connective Tissue Disorders: Recognizing and Treating Structural Defects
(National Institutes of Health)
Your body’s connective tissues, like tendons and ligaments, help your joints move. They also give structure and flexibility to skin, blood vessels, and ... - What Are the Symptoms of Fragile X Syndrome?
(Eunice Kennedy Shriver National Institute of Child Health and Human Development)
Fragile X Syndrome/Symptoms ... Fragile X Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ... - Fragile X-Associated Disorders (FXD): A Handbook for Families, Health Care Providers, Counselors, and Educators (National Fragile X Foundation) - PDFFragile X Syndrome/Start Here ... Fragile X Syndrome ... National Fragile X Foundation ... PDF ... fragile x, handbook, 3rd edition, NFXF
- Guide to Understanding Apert Syndrome (Children's Craniofacial Association) - PDFCraniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
- Bell's Palsy (Mayo Foundation for Medical Education and Research)Bell's Palsy/Start Here ... Bell's Palsy ... Mayo Foundation for Medical Education and Research
- Movement Symptoms (Parkinson's Foundation)Parkinson's Disease/Symptoms ... Parkinson's Disease ... Parkinson's Foundation ... Know the movement symptoms Parkinson's can cause such as tremors, postural instability, ...
- Eye Movement Disorders/Genetics ... Eye Movement Disorders ... National Human Genome Research Institute ... Duane syndrome is a rare, congenital eye movement disorder.