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Congenital Insensitivity to Pain with Anhidrosis Syndrome: A Case Report
(Galenos Yayincilik, 2014) Turan, Hakan; Besir, Fahri Halit; Uslu, Esma; Basar, Feyza; Gun, Emrah; Gecer, Yavuz
Congenital Insensitivity to Pain with Anhidrosis syndrome is a rare, autosomal recessively inherited syndrome caused by neurotrophic tyrosine receptor kinase 1 gene mutation. The basic findings of the syndrome are absence of pain sense, anhidrosis, and self-destructive behaviors. Herein, we describe a 4-year-old boy presented with xerosis, anhidrosis, and traumatic lesions on the hands and diagnosed as Congenital Insensitivity to Pain with Anhidrosis syndrome. On the occasion of this case, we aimed to review general and dermatological characteristics of this rare syndrome.
Prurigo Pigmentosa: A Case Report
(Galenos Yayincilik, 2013) Turan, Hakan; Acer, Ersoy; Albayrak, Hulya; Uslu, Esma; Ayaz, Nusret; Basar, Feyza; Aliagaoglu, Cihangir
What is your diagnosis 1?
(Deri Zuhrevi Hastaliklar Dernegi, 2015) Turan, Hakan; Uslu, Esma; Yavuzcan, Gizem; Basar, Feyza; Erdem, Havva
What is your diagnosis 1?
(Deri Zuhrevi Hastaliklar Dernegi, 2015) Turan, Hakan; Uslu, Esma; Erdem, Havva; Basar, Feyza