Address correspondence to Melinda R. Mohr, M.D., Eastern Virginia Medical School, Department of Dermatology, 721 Fairfax Avenue, Suite 200, Norfolk, VA 23507, USA, or e-mail: [email protected].

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Abstract

Abstract: We present two rare cases of phacomatosis pigmentovascularis type IIb, with one patient demonstrating concurrent Sturge–Weber syndrome and Klippel–Trenaunay syndrome. To the best of our knowledge, this is the second infantile case meeting diagnostic criteria for systemic phacomatosis pigmentovascularis type IIb, Sturge–Weber syndrome and Klippel–Trenaunay syndrome in the English language literature.

References

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Volume27, Issue3

May/June 2010

Pages 303-305

Two Reports of Phacomatosis Pigmentovascularis Type Iib, One in Association with Sturge–Weber Syndrome and Klippel–Trenaunay Syndrome

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Two Reports of Phacomatosis Pigmentovascularis Type Iib, One in Association with Sturge–Weber Syndrome and Klippel–Trenaunay Syndrome

Abstract

References

Citing Literature

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