Carnitine Palmitoyltransferase Deficiency
Newsletter for health care professionals and patients interested in CPT deficiency, a mitochondrial disorder of fat metabolism that causes muscle breakdown.
Children Living with Inherited Metabolic Diseases (CLIMB)
national umbrella organization working on behalf of children, young people, and adults affected by metabolic diseases.
Children's PKU Network
working to maintain an agenda of public awareness, education, and direct assistance to help people with PKU and other metabolic disorders.
Homocystinuria Support
provides information about the illness, recommended diet, and links.
Nonketotic Hyperglycinemia
hyperglycinemia (nkh) parent network.
Parents of Galactosemic Children, Inc.
Information about galctosemia and a resource for families living with galactosemia.
Spiral Notebook: Carnitine Palmitoyl Transferase Deficiency
a newsletter about a rare genetic disorder of fat metabolism that causes muscle breakdown.
United Mitochondrial Disease Foundation
To promote research for the cure and treatment, and to provi
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