Dr. Kendall's conditions and procedures:

Adrenoleukodystrophy, Autosomal, Neonatal Form

Angelman Syndrome

Arginase Deficiency

Arginine-Glycine Amidinotransferase Deficiency

Arginninosuccinic Acid Synthetase Deficiency

Autism

Biotinidase Deficiency

Canavan Disease

Carbamoyl - Phosphate Synthase 1 Deficiency

Carbohydrate Deficiency Glycoprotein Syndrome, Type II

Carnitine Deficiency

Carnitine Transport Deficiency

Carnitine-Acylcarnitine Translocase Deficiency

Citrulline Transport Defect

Citrullinemia

Citrullinemia II

Drug-Induced Myopathies

Duchenne Muscular Dystrophy

Fabry's Disease

Fragile X Syndrome

Galactosemia

Genetic Diseases

Glucocerebrosidase Deficiency

Glycogen Storage Disease

Hemochromatosis

Homocarnosinosis

Inborn Errors of Metabolism

Krabbe Disease

Late-Onset Argininosuccinase Lyase Deficiency

Late-Onset Citrullinemia

Leigh Syndrome

McArdle Disease

Medium-Chain Acyl-CoA Dehydrogenase Deficiency

MELAS

Menkes Disease

Metabolic Disorders

Metabolic Myopathies

Metachromatic Leukodystrophy

Methylmalonic Academia

Mitochondrial Diseases

Mitochondrial Encephalomyopathy - Aminoacidopathy

Mitochondrial Myopathy - Lactic Acidosis

Mitochondrial Neurogastrointestinal Encephalopathy Syndrome

Mitochondrial Trifunctional Protein Deficiency

Neonatal Argininosuccinase Lyase Deficiency

Physical Examination

Pompe Disease

von Gierke's Disease

X-Linked, Angelman-Like Syndrome