International Journal of Health and Clinical Research
A Rare Case Report of Garcia Hafner Happle Syndrome
Yazarlar: Lisa Jennifer Dsouza, Oudeocoumar P, Jude E Dileep, Rajkiran Thakarya, Ilakkia Priya Sadasivam
Cilt 4 , Sayı 17 , 2021 , Sayfalar 245-246
Konular:-
Anahtar Kelimeler:Garcia Hafner Happle Syndrome,Isorder
Özet: 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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BibTex
KOPYALA
@article{2021, title={A Rare Case Report of Garcia Hafner Happle Syndrome}, volume={4}, number={245–246}, publisher={International Journal of Health and Clinical Research}, author={Lisa Jennifer Dsouza,Oudeocoumar P,Jude E Dileep,Rajkiran Thakarya,Ilakkia Priya Sadasivam}, year={2021} }
APA
KOPYALA
Lisa Jennifer Dsouza,Oudeocoumar P,Jude E Dileep,Rajkiran Thakarya,Ilakkia Priya Sadasivam. (2021). A Rare Case Report of Garcia Hafner Happle Syndrome (Vol. 4). Vol. 4. International Journal of Health and Clinical Research.
MLA
KOPYALA
Lisa Jennifer Dsouza,Oudeocoumar P,Jude E Dileep,Rajkiran Thakarya,Ilakkia Priya Sadasivam. A Rare Case Report of Garcia Hafner Happle Syndrome. no. 245–246, International Journal of Health and Clinical Research, 2021.