A Rare Case Report of Garcia Hafner Happle Syndrome

Lisa Jennifer Dsouza; Oudeocoumar P; Jude E Dileep; Rajkiran Thakarya; Ilakkia Priya Sadasivam

A Rare Case Report of Garcia Hafner Happle Syndrome

Authors

Lisa Jennifer Dsouza 2nd Year Post-Graduate, Department of Dermatology, Venereology and Leprosy, Aarupadai Veedu Medical College and Hospital, Puducherry, India
Oudeocoumar P Professor and Head, Department of Dermatology, Venereology and Leprosy, Aarupadai Veedu Medical College and Hospital, Puducherry, India
Jude E Dileep Assistant Professor, Department of Dermatology, Venereology and Leprosy, Aarupadai Veedu Medical College and Hospital, Puducherry, India
Rajkiran Thakarya 2nd Year Post-Graduate, Department of Dermatology, Venereology and Leprosy, Aarupadai Veedu Medical College and Hospital, Puducherry, India
Ilakkia Priya Sadasivam 2nd Year Post-Graduate, Department of Dermatology, Venereology and Leprosy, Aarupadai Veedu Medical College and Hospital, Puducherry, India

Keywords:

Garcia Hafner Happle Syndrome,disorder

Abstract

Garcia Hafner Happle Syndrome is a rare type of epidermal nevus syndrome. It is caused by mutations to the fibroblast growth factor receptor 3 (FGFR) gene and is also called FGFR3 epidermal nevus syndrome. It is clinically characterized by keratinocytic epidermal naevii with cerebral and skeletal involvement.

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Published

2021-09-30

How to Cite

Lisa Jennifer Dsouza, Oudeocoumar P, Jude E Dileep, Rajkiran Thakarya, & Ilakkia Priya Sadasivam. (2021). A Rare Case Report of Garcia Hafner Happle Syndrome. International Journal of Health and Clinical Research, 4(17), 245–246. Retrieved from https://ijhcr.com/index.php/ijhcr/article/view/2820