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Learning Genetics
Learning Genetics-Home
Understanding genetics
Patterns of inheritance
Family history
Genetic testing and screening
Ethical, legal and social implications of genetics
Communicating genetic information
Common genetic conditions
GP Associates in Training - Genetics in Primary Care
Genetics Clinical Services
Glossary
Teaching Genetics
Teaching Genetics-Home
Medical Practitioners
Medical Students
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GP Specialty Registrars
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Non-genetics specialty trainees
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Nursing Professions
Genetic Education Framework
Team Publications
Pharmacogenetics
Explanation of terms
Key publications
Commentary
Pharmacogenetics
Websites and e-learning
Why should health professionals be interested in pharmacogenetics?
Reusable Learning Resources: The Genomic Basis of Therapeutics
Dietitians
Learning about genetics
Genetics in the BDA curriculum
Genetic activities in dietetic practice
Dietetic Resources
Dietitians and "Telling stories"?
Key publications
Websites and e-learning
Glossary
Family Tree
Genetics in Practice
Genetics in Practice-Home
Genetic Activities in Clinical Practice
Workforce competences
Competence Framework
Developing Services and New Roles
Service development initiatives - mainstreaming genetics
A Toolkit for developing new services
How the Toolkit was developed
Clinical Questions
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Learning Genetics
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Common genetic conditions
>> Becker muscular dystrophy
Becker muscular dystrophy
(see Duchenne muscular dystrophy)
Back to genetic conditions index
Learning Genetics
Learning - Home
Understanding genetics
Patterns of inheritance
Family history
Genetic testing and screening
Ethical, legal and social implications of genetics
Communicating genetic information
GP Associates in Training - Genetics in Primary Care
Common genetic conditions
Achondroplasia
Adult polycystic kidney disease
Albinism (oculocutaneous)
Alpha-thalassaemia
Autosomal recessive polycystic kidney disease
Becker muscular dystrophy
Beta-thalassaemia
Charcot-Marie-Tooth disease
Congenital adrenal hyperplasia (21-hydroxylase deficiency)
Congenital sensorineural deafness
Cystic fibrosis
Down syndrome
Duchenne muscular dystrophy
Edwards Syndrome
Familial Adenomatous Polyposis
Familial Hypercholesterolaemia (FH)
Fragile X Syndrome
Friedreich Ataxia
Glucose-6-Phosphate Dehydrogenase Deficiency
Haemophilia A
Hereditary Haemochromatosis
Huntington Disease
Hypertrophic Cardiomyopathy
Inborn Errors of Metabolism
Klinefelter Syndrome
Marfan Syndrome
Mitochondrial Disorders
Muscular Dystrophy
Myotonic Dystrophy
Neurofibromatosis Type 1
Osteogenesis Imperfecta
Patau Syndrome
Phenylketonuria
Polycystic Kidney Disease
Retinitis Pigmentosa
Rett Syndrome
Sickle Cell Disease
Spinal Muscular Atrophy
Tay-Sachs Disease
Tourette Syndrome
Triple X Syndrome
Tuberous Sclerosis Complex
Turner Syndrome
Wilson Disease
47, XYY
Cerebral Palsy
Cleft Lip and Palate
Congenital Heart Disease
Coronary Artery Disease
Diabetes
Epilepsy
Learning Disabilities
Manic Depression
Neural Tube Defects: Anencephaly and Spina Bifida
Schizophrenia
Cousin Marriage
Maternal Age Effect
Recurrent Miscarriages
Genetics Clinical Services
Glossary