Domains targeting keyword genetic disorder

Fabry disease is a rare genetic disorder and a life-threatening condition. Learn about the signs, symptoms, inheritance, genetics, and treatment.

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

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.

Are you seeking genetic testing for children with autism spectrum disorder or developmental delay? Lineagen is the expert in providing comprehensive genetic testing for children with neurodevelopmental concerns.

বাংলাদেশের সব খবর সহ পুরো বিশ্বের সাম্প্রতিক খবর দেখুন এবং উত্তরার খবর ও ঢাকার খবর এবং বাংলাদেশ ও আন্তর্জাতিক সংবাদ জানুন সবার আগে

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.

Neurofibromatosis is the most common genetic neurological disorder. Neurofibromatosis (NF) has been classified into two distinct types: NF1 and NF2. Neurofibromatosis 1 (NF1), also known as von Recklinghausen NF or Peripheral NF, occurring in 1:3,500 births, is characterized by multiple cafe-au-lait spots and neurofibromas on or under the skin. Enlargement and deformation of bones and…

The Canavan Foundation is a not-for-profit organization that was founded in 1992 by the parents and friends of children affected by the Canavan disease.

Extensive Information on Pain, Pain Management, Sports Injuries, Manual Therapy, Alternate Therapy, Find Pain Physician and Chiropractors, and Pain Discussion Board @ ePainAssist!

Gaucher disease is a genetic disorder and affects the body's organs and tissues. Learn about Gaucher disease symptoms, testing and treatments.

Alexander L. Shifrin, MD - Endocrine Surgery, Jersey Shore Medical Center, State Route 33, Neptune, New Jersey (NJ) 07754; Phone (732) 776-4770; Fax (732) 776- 3763, Center for PARATHYROID, THYROID and ADRENAL SURGERY at Jersey Shore University Medical Center<br /> Alexander L. Shifrin,MD,FACS,FACE,ECNU Surgical Director, Meridian Thyroid, Parathyroid and Adrenal Center.<br /> EDUCATION AND TRAINING, Clinical Interests: minimally invasive thyroid, parathyroid and adrenal surgery, Practice in News and Press Release. Center for PARATHYROID, cenetr of THYROID, center for ADRENAL SURGERY. Alexander Shifrin, MD, FACS, FACE, NCNU

The CGD Society - supporting families affected by chronic granulomatous disorder, a rare genetic condition that affects the immune system.

Mitochondrial disease is a chronic, genetic disorder. The Abel Foundation helps the families & sufferers of mitochondrial disease

Hemochromatosis is a genetic metabolic disorder of excess iron absorption and too much iron storage in the body. Find the diet & supplement help you need

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.

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

The Wilson Disease Association (WDA) is a volunteer organization striving to promote the well being of patients with Wilson disease and their families and friends.

Genomind is a personalized medicine company bringing innovation to mental healthcare through genetic testing.

Celiac disease or “CD” is a common genetic disorder that affects millions of people in the United States. Yet this condition often goes diagnosed...