Full Text Journal Articles by
Author Elif Soyak Aytekin

Advertisement

Find full text journal articles








A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess.

Elif Soyak Aytekin, Oguzhan Serin, Deniz Cagdas, Cagman Tan, Tekin Aksu, Yagmur Unsal, Selma Yeni, Diclehan Orhan, Zeynep Alev Ozon, Ilhan Tezcan,

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) (polyglandular endocrinopathy type 1) is a rare autosomal recessive disorder caused by mutations in the autoimmune regulator gene (AIRE). The major clinical features of APECED are hypoparathyroidism, adrenal insufficiency (Addison disease), and chronic mucocutaneous candidiasis. This disease is also associated with multiple other and uncommon autoimmune ... Read more >>

Pediatr Infect Dis J (The Pediatric infectious disease journal)
[2021, 40(1):66-69]

Cited: 0 times

View full text PDF listing >>



In case of recurrent wheezing and bronchiolitis: Think again, it may be a primary immunodeficiency.

Begum Ozbek, Deniz Çağdaş Ayvaz, Saliha Esenboga, Sevil Oskay Halaçlι, Elif Soyak Aytekin, Ismail Yaz, Çağman Tan, Ilhan Tezcan,

BACKGROUND:Wheezing, starting early in life, is a heterogeneous medical condition caused by airway obstruction due to different underlying mechanisms. Primary immunodeficiencies are also among the risk factors that cause wheezing and recurrent bronchiolitis. ADA deficiency is a primary immunodeficiency, also a rare metabolic disease associated with multisystemic clinical findings. OBJECTIVE:This ... Read more >>

Asian Pac J Allergy Immunol (Asian Pacific journal of allergy and immunology)
[2019, :]

Cited: 0 times

View full text PDF listing >>



Advertisement

Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency.

Ismail Solmaz, Elif Soyak Aytekin, Deniz Çağdaş, Cagman Tan, Ilhan Tezcan, Rahsan Gocmen, Goknur Haliloglu, Banu Anlar,

Defects in the regulatory components of the complement system can lead to inflammatory diseases. We present a patient who had four episodes of demyelination in the central nervous system as the only manifestation of inherited CD59 deficiency. Relapsing encephalopathy partially responsive to intravenous immunoglobulin and steroid treatments on the background ... Read more >>

Neuropediatrics (Neuropediatrics)
[2020, 51(3):206-210]

Cited: 0 times

View full text PDF listing >>





Advertisement

Disclaimer
0.4686 s