HLAs in children with minimal change disease and other types of nephrotic syndrome in the Southern Part of Turkey

HLAs in children with minimal change disease and other types of nephrotic syndrome in the Southern Part of Turkey

The aim of this study was to investigate the human leukocyte antigen (HLA) profile of children with nephrotic syndrome in the southern part of Turkey. Seventy-eight children with nephrotic syndrome were studied for the frequency of class I and class II human leukocyte antigens. Forty-seven of them were steroid sensitive nephrotic syndrome (minimal change disease-MCD) and 31 were other types of nephrotic syndrome. The results were compared with 133 healthy subjects for HLA groups. HLA B13, Cw5, Cw7, DR4, DR7, DRw10, Drw15(2) and DQ2 in the MCD group and HLA A31, B8, B13, B17, Cw2, Cw6, Cw7, DRw10 and DRw12 in the non-MCD group were found significantly increased when compared to healthy controls. MCD patients with frequent relapses had higher frequencies of both Cw6 and DR1 (p < 0.005) and MCD patients with infrequent relapses had a higher frequency of Cw7 (p < 0.05). In conclusion, HLA groups may help in the early diagnosis of these variants.

___

Turkish Journal of Pediatrics-Cover
  • ISSN: 0041-4301
  • Yayın Aralığı: Yılda 6 Sayı
  • Başlangıç: 1958
  • Yayıncı: Hacettepe Üniversitesi Çocuk Sağlığı Enstitüsü Müdürlüğü
Sayıdaki Diğer Makaleler

Chronic inflammatory bowel disease in a patient with common variable immunodeficiency

Raşit Vural YAĞCI, Sema AYDOĞDU, Güzide AKSU, Berhan GENÇ, Necil KÜTÜKÇÜLER

Prevalence of asthma-associated symptoms in Turkish children

İpek TÜRKTAŞ, Z. Toros SELÇUK, A. Fuat KALYONCU

MR imaging of pelvic and thigh muscles in congenital muscular dystrophy

Beril TALİM, Nuri BAŞGÜN, Haluk TOPALOĞLU, Ergun KARAAĞAOĞLU, Üstün AYDINGÖZ, Aytekin OTO

The role of pulmonary artery anatomy in repair of tetralogy of fallot

A. Şükrü MERCAN, Atilla SEZGİN, Atılay TAŞDELEN, Coşkun İKİZLER, Kürşad TOKEL, Enver EKİCİ, Sait AŞLAMACI

Transcatheter closure of secundum atrial septal defects, a ventricular septal defect, and a patent arterial duct

Arman BİLGİÇ, Alpay ÇELİKER, Süheyla ÖZKUTLU, Tevfik KARAGÖZ, Canan AYABAKAN

Pseudohypoparathyroidism type IA and II with severe neuropsychic manifestations

Stepan KUTILEK, Pavel KABICEK, Jara NEDVIDKOVA, Milan BAYER

Combined use of chemotherapy and 131 I-metaiodobenzylguanidine in the treatment of advanced-stage neuroblastoma.

Oktay SARI, Canan AKYÜZ, Suna EMİR, Ömer UĞUR

Pediatricians' opinions about the problems between the departments of pediatrics and child psychiatry and possible solutions

S. Ebru ÇENGEL, Z. Bengi SEMERCİ

Systemic lupus erythematosus presenting with generalized lymphadenopathy : A case report

Betül BİNER, Serap KARASALİHOĞLU, Betül ACUNAŞ, Ülfet VATANSEVER

Noninvasive diagnosis and surgical management in total anomalous pulmonary venous return draining into the coronary sinus: Report of 2 cases

Bekir KAYHAN, Vedide TAVLI, Mustafa KIRMAN, Mehmet TEKDOĞAN, F. Fevzi OKUR