Websites targeting keyword genetic syndrome

Atypical hemolytic-uremic syndrome (aHUS) is a genetic disease associated with chronic risk of complement-mediated, systemic thrombotic microangiopathy.

The Usher Syndrome Coalition raises awareness and accelerates research for the most common genetic cause of combined deafness and blindness.

Hunter Syndrome (MPS II) is a serious genetic disorder that primarily affects males. People with MPS II lack an enzyme that breaks down mucopolysaccharides.

Helping Hands’ mission is to help developmentally delayed preschoolers prepare for public education.

FG Syndrome is an X-linked genetic syndrome, believed to affect both boys and girls; which causes a variety of physical anomolies, developmental delays, and special health needs.

MPS ~ ML Forum is dedicated to bringing families of children affected by Mucopolysaccharidoses and Mucolipidoses together on the internet.

Dr.Amy Burkhart-an integrative physician & dietitian.Medical expert in digestive health & nutrition. Gluten Sensitivity & Celiac specialist.

Chromosome Disorder Outreach, Inc. (CDO) is a non-profit organization for families affected by any type of rare chromosome disorder: deletions, translocations, trisomies, rings and inversions.

Genetics and Disabilities Diagnostic Care Center specializes in the dignosis and treatment of Down Syndrome, Autism and Metabolic Disorders. Information on Targeted Nutritional Intervention treatments and Secretin therapies.

Tourette Syndrome Association of Australia is a non-profit, self-funded, registered charity run by volunteers — consisting of people with TS, their families, health and education professionals and other interested and concerned people. The association disseminates educational materials in the fields of health care, education and welfare service. We support parent advocacy and other services to help families manage TS.

Methylation Genetics Expert Nancy Mullan, MD - Autism Spectrum Disorders, Women's Health, Psychological Disorders, Thyroid Disorders

Our goal is to provide diagnostic solutions to meet unmet needs within gut dysbiosis diagnostics. Microbiota were rated among the world 10th most promising investment objects in 2013.

The NIFTY Test is a non-invasive prenatal test (NIPT), which safely screens for genetic conditions like Down Syndrome, from week 10 of pregnancy.

Sickle cell and Young Stroke Survivors is a charity that support children and young people living with Sickle cell Anaemia and one of it devastating complications childhood stroke and Moyamoya syndrome.

A Simply Enchanted Life is a look into the life of a mommy, book freak, photographer, artisan of high quality-handcrafted soap, self proclaimed nerd and jedi. The most important thing in life to me is family. I am the mom of six precious children and I work hard at caring for their needs. This can be a challenge because several members of our family have a genetic condition called Ehlers-Danlos Syndrome. We invite you to take a peek at our honest book,recommendations and discussions, learn about our health challenges and take a peek at our handcrafted soap!

<p><i>Cardiovascular Diabetology</i> considers manuscripts on all aspects of the diabetes/cardiovascular interrelationship and the metabolic syndrome; this includes clinical, genetic, experimental, pharmacological, epidemiological and molecular biology research.</p>

WarmLine Family Resource Center - Supporting families who have children with disabilities and special healthcare needs from birth to adulthood.