Genetics – Clinical & Metabolic

General Genetic Information

Syndromes without a Name – SWAN

Resources

Support Groups – Disease Specific

Accommodating Children with Special Dietary Needs in the School Lunch Programs

Angelman Syndrome

Biotinidase Deficiency

Chromosome Disorders

Congenital Adrenal Hyperplasia

Craniofacial Abnormalities and Syndromes

Cri du Chat  (5p- Syndrome)

Down Syndrome

Dwarfism and Short Stature

Ehlers-Danlos Syndrome

 Fatty Acid Oxidation Disorders

 Fragile X Syndrome

 Galactosemia

 Glycogen Storage Diseases

Hereditary Cancer Syndrome Support Groups

Huntington Disease

Klinefelter Syndrome

Maple Syrup Urine Disease

Marfan Syndrome

Mitochondrial Diseases

Mucopolysaccharidoses

Muscular Dystrophy

 Neurofibromatosis Type 1 and 2

Organic Acidemias

Osteogenesis Imperfecta

Phenylketonuria (PKU)

 Prader Willi Syndrome

Propionic Acidemia

Rett Syndrome

Turner Syndrome

Urea Cycle Disorders

Velocardiofacial Syndrome or Deletion Chromosome 22q11 Support Groups

 Wolf-Hirschhorn Syndrome (4p- Syndrome)