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Exoming into Rare Skin Disease: EGFR Deficiency

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Presentation on theme: "Exoming into Rare Skin Disease: EGFR Deficiency"— Presentation transcript:

1 Exoming into Rare Skin Disease: EGFR Deficiency
Matthew A. Brooke, Edel A. O'Toole, David P. Kelsell  Journal of Investigative Dermatology  Volume 134, Issue 10, Pages (October 2014) DOI: /jid Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 An illustration of EGFR ligand shedding and the interactions of EGFR ligands with members of the ErbB receptor tyrosine kinase family, ErbB1 (EGFR), and ErbB4. Dimerization of ErbB1 with ErbB2 is shown for representative purposes; numerous other receptor homodimers and heterodimers can be formed. AREG, amphiregulin; BTC, betacellulin; EPGN, epigen; EREG, epiregulin; HB-EGF, heparin-binding EGF; TGFα, transforming growth factor-α. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 Hypotrichosis of the eyebrows, trichomegaly, and folliculitis in a patient with ADAM17 deficiency. Image published with patient's consent. Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Journal of Investigative Dermatology 2014 134, 2486-2488DOI: (10
Journal of Investigative Dermatology  , DOI: ( /jid ) Copyright © 2014 The Society for Investigative Dermatology, Inc Terms and Conditions


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