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Dec 20, 2009

Genetics and Birth Defects (Source:NIH)

Abnormalities see Birth Defects

Achondroplasia see Dwarfism

Acid Maltase Deficiency see Metabolic Disorders

Adrenoleukodystrophy see Leukodystrophies

Alpha-1 Antitrypsin Deficiency

Anencephaly see Neural Tube Defects

Arnold-Chiari Malformation see Head and Brain Malformations

Birth Defects

Brain Malformations see Head and Brain Malformations

Canavan Disease see Leukodystrophies

Cerebral Palsy

Charcot-Marie-Tooth Disease

Cleft Lip and Palate

Congenital Heart Disease

Cystic Fibrosis

Dandy-Walker Syndrome see Head and Brain Malformations

Down Syndrome

Duchenne Muscular Dystrophy see Muscular Dystrophy

Dwarfism

Ehlers-Danlos Syndrome

Family History

Fetal Alcohol Syndrome

Fragile X Syndrome see Genetic Disorders

Gaucher's Disease

Genes

Genetic Brain Disorders

Genetic Disorders

Genetic Testing/Counseling

Head and Brain Malformations

Hemochromatosis

Hemophilia

Human Genome Project see Genes

Huntington's Disease

Hydrocephalus

Hypermobility Syndrome see Ehlers-Danlos Syndrome

Klinefelter Syndrome

Leukodystrophies

Marfan Syndrome

Menkes Syndrome

Metabolic Disorders

Mucopolysaccharidoses see Metabolic Disorders

Muscular Dystrophy

Neural Tube Defects

Neurofibromatosis

Osteogenesis Imperfecta

Personalized Medicine

Phenylketonuria

PKU see Phenylketonuria

Prader-Willi Syndrome

Rare Diseases

Sickle Cell Anemia

Spina Bifida

Spinal Muscular Atrophy

Tay-Sachs Disease

Tourette Syndrome

Tuberous Sclerosis

Turner's Syndrome

von Recklinghausen's Disease see Neurofibromatosis

Wilson's Disease

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