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© 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare
www.geneticseducation.nhs.uk
Clinical photographs of genetic conditions
This PowerPoint file contains a number of slides that may be useful for teaching of
genetics concepts.
You may use these slides and their contents for non-commercial educational purposes.
© 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare
www.geneticseducation.nhs.uk
Fig. Disease box 9 ©Scion Publishing Ltd
Clinical features of Rubinstein-Taybi syndrome
(a) The typical face, (b) broad thumb, and (c) characteristic appearance of large toes.
© 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare
www.geneticseducation.nhs.uk
Fig. 7.2 ©Scion Publishing Ltd
Photo. courtesy of Dr Jill Clayton-Smith
A 10-year-old girl with Angelman syndrome. She has a mutation in the UBE3A gene.
© 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare
www.geneticseducation.nhs.uk
Fig. 7.3 ©Scion Publishing Ltd
A baby with Prader-Willi syndrome. Note the marked hypotonia

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Clinical Photos - Other Genetic conditions.

  • 1. © 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare www.geneticseducation.nhs.uk Clinical photographs of genetic conditions This PowerPoint file contains a number of slides that may be useful for teaching of genetics concepts. You may use these slides and their contents for non-commercial educational purposes.
  • 2. © 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare www.geneticseducation.nhs.uk Fig. Disease box 9 ©Scion Publishing Ltd Clinical features of Rubinstein-Taybi syndrome (a) The typical face, (b) broad thumb, and (c) characteristic appearance of large toes.
  • 3. © 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare www.geneticseducation.nhs.uk Fig. 7.2 ©Scion Publishing Ltd Photo. courtesy of Dr Jill Clayton-Smith A 10-year-old girl with Angelman syndrome. She has a mutation in the UBE3A gene.
  • 4. © 2009 NHS National Genetics Education and Development Centre Genetics and Genomics for Healthcare www.geneticseducation.nhs.uk Fig. 7.3 ©Scion Publishing Ltd A baby with Prader-Willi syndrome. Note the marked hypotonia