Cowden disease | About the Disease | GARD - Genetic and Rare …
Cowden disease is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing.
Cowden syndrome - About the Disease - Genetic and Rare …
Cowden disease; Multiple hamartoma syndrome Cowden disease; Multiple hamartoma syndrome. Read More . Read Less . About the Disease ; Getting a Diagnosis ; Resources and Support ; Disease at a Glance; Symptoms; Causes; Find Your Community; Participating in Clinical Studies; Navigate to sub-section.
Lhermitte-Duclos disease | About the Disease | GARD - Genetic …
RARe-SOURCE™ offers rare disease gene variant annotations and links to rare disease gene literature. GeneReviews provides clinical information on genetic diseases, including diagnosis, treatment, and genetic counseling.
Cowden syndrome - About the Disease - Genetic and Rare …
Cowden disease; Multiple hamartoma syndrome Cowden disease; Multiple hamartoma syndrome. Read More . Read Less . About the Disease ; Getting a Diagnosis ; Living With the Disease ; Disease at a Glance; Symptoms; Causes; Advocacy and Support Groups; Participating in Clinical Studies; Navigate to sub-section.
Síndrome de Cowden | Sobre la enfermedad | GARD - Genetic and …
El síndrome de Cowden es una enfermedad hereditaria que se caracteriza por tumores múltiples, no cancerosos (llamados hamartomas) en varias partes del cuerpo. Los síntomas comienzan, por lo general, antes de los 30 años, e incluyen cabeza grande (macrocefalia), tumores benignos del folículo piloso , y ampollas blancas con una superficie ...
Adiposis dolorosa | About the Disease | GARD - Genetic and Rare ...
The National Organization for Rare Disorders (NORD) maintains a list of rare disease centers with experts that work together to find treatments and cures for a broad range of rare diseases. Search NORD's Center Directory to find experts near you.
Contact GARD - National Institutes of Health
GARD defines a patient organization as one that creates a community of support by connecting people living with the same rare disease, their families, and caregivers to others like them. At minimum, all organizations submitting this form should meet the following criteria:
Contact GARD - National Institutes of Health
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