Ara
Toplam kayıt 8, listelenen: 1-8
Vulvar Dermatoses
(Galenos Yayincilik, 2017)
Vulvar dermatoses are seen commonly. However, unique anatomical and physiological structure of vulva makes it difficult to diagnose and treat. Detailed history and careful physical examination is very crucial in diagnosis ...
Az bilinen bir konu Delüzyonel Parazitoz: Bir olgu sunumu
(2020)
Delüzyonel parazitoz (DP) tıbbi bir kanıt olmamasına rağmen ki?inin parazit ya da ya?ayan küçük yaratıklar tarafından enfekte olduğu yanlı? ve ısrarlı inancı ile seyreden sanrısal bir bozukluktur. DP yüzyıldan uzun zamandır ...
Hypertrichosis in Childhood
(Galenos Yayincilik, 2018)
Hypertrichosis is more than normal and excessive hair growth according to individual's age and sex. in hypertrichosis, hair growth is not androgen dependent and does not include male type hair growth. Hypertrichosis ...
Dermatological manifestations of autoinfammatory diseases in children
(Turkish Society of Hematology, 2014)
Autoinflammatory diseases include a group disease characterized by recurrent systemic inflammatory attacks due to failure in the regulation of the innate immune system. In contrast to autoimmune diseases absence of ...
Clinical, demographic and laboratory features of children with alopecia areata
(Turkish Society of Hematology, 2014)
Objective: Alopecia areata (AA) is an inflammatory skin disease with an unknown etiology and characterized by loss of hair without scar formation. In this study we aimed to investigate the clinical and demographic ...
Cutaneous manifestations of endocrine disorders
(2011)
During the course of endocrine diseases, skin symptoms may be seen. Recognition of endocrin skin lesions have very important role in the diagnosis and treatment of endocrine diseases. In this study, we aimed to investigate ...
Phacomatosis pigmentovascularis
(2012)
Phacomatosis pigmentovascularis is a rare genodermatosis which consists of a combination of melanocytic nevi and vascular malformations. Although the classification of phacomatosis pigmentovascularis is updated, recently ...
Hereditary sensory and autonomic neuropathy type I: A case presenting with acral neuropathic ulcers
(Turkiye Klinikleri, 2012)
Hereditary sensory and autonomic neuropathies; are a group of genetic disorders characterized by pain insensitivity, normal muscle capacity and reflexes with acral trophic ulcers, deformities and osteomyelitis. In the ...