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akaturk Akademik ölçüm

Makale detayı · 2024

17α Hydroxylase/17,20 lyase deficiency: clinical features and genetic insights from a large Turkey cohort

Endocrine

YÖKSİS OpenAlex Açık erişim · hybrid SJR Q2 JCR Q2 Atıf 14 Yüzdelik 87.7% FWCI 2.12
Yıl
2024
ISSN
1355-008X
Tür
article

Veri kaynağı ayrımı

  • YÖKSİS YÖKSİS makale kaydı
  • OpenAlex OpenAlex zenginleştirmesi (özet, atıf, konular)

Özet

İngilizce (OpenAlex)

PURPOSE: 17α Hydroxylase/17,20 lyase deficiency (17OHD) is a rare form of congenital adrenal hyperplasia, typically diagnosed in late adolescence with symptoms of pubertal delay and hypertension. This study aimed to determine the clinical and laboratory characteristics of 17OHD cases and gather data on disease management. METHODS: Data from 97 nationwide cases were analyzed using the CEDD-NET web system. Diagnostic, follow-up findings, and final heights of patients were evaluated. RESULTS: Mean age at admission was 13.54 ± 4.71 years, with delayed puberty as the most common complaint. Hypertension was detected in 65% at presentation; hypokalemia was present in 34%. Genetic analysis revealed Exon 1-6 homozygous deletion as the most frequent mutation, identified in 42 cases. Hydrocortisone replacement was universal; pubertal replacement was administered to 66 cases. Antihypertensive treatment was required in 57 (90%) patients. Thirty-seven cases reached final height, with an average SD of 0.015 in 46,XX and -1.43 in 46,XY. Thelarche and pubarche did not develop properly in some cases despite estradiol treatment. CONCLUSION: This study represents the largest cohort of pediatric cases of 17-hydroxylase deficiency (17OHD) documented in the literature. Hypertension and hypokalemia can serve as guiding indicators for early diagnosis.The final height is typically considered to be normal. The relationship between genotype and phenotype remains elusive. The initial genetic test for exon 1-6 deletions may be MLPA in our region.

Konular

  • Sexual Differentiation and Disorders
  • Metabolism and Genetic Disorders
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Birincil konu Sexual Differentiation and Disorders

Yazarlar

  1. ZEYNEP ŞIKLAR ANKARA ÜNİVERSİTESİ
  2. EMİNE ÇAMTOSUN
  3. SEMİH BOLU
  4. MELEK YILDIZ
  5. AYŞEHAN AKINCI
  6. FİRDEVS BAŞ
  7. İSMAİL DÜNDAR
  8. ASLI BEŞTAŞ
  9. EDİP UNAL
  10. PINAR KOCAAY
  11. TÜLAY GÜRAN
  12. GÖNÜL BÜYÜKYILMAZ
  13. AYLİN KILINÇ UĞURLU
  14. BUŞRA GÜRPINAR TOSUN
  15. AHMET İHSAN TURAN
  16. ERDAL KURNAZ
  17. BİLGİN YÜKSEL
  18. DOĞA TÜRKKAHRAMAN
  19. ATİLLA ÇAYIR
  20. GAMZE ÇELMELİ
  21. ELMAS NAZLI GÖNÇ
  22. BERAY SELVER EKLİOĞLU
  23. SEMRA ÇETİNKAYA
  24. SENİHA KİREMİTÇİ YILMAZ
  25. MEHMET EMRE ATABEK
  26. MUAMMER BÜYÜKİNAN SELÇUK ÜNİVERSİTESİ
  27. EMRULLAH ARSLAN
  28. EDA MENGEN UÇAKTÜRK
  29. ESRA DENİZ PAPATYA ÇAKIR
  30. MURAT KARAOĞLAN
  31. NİHAL HATİPOĞLU
  32. ZERRİN ORBAK ATATÜRK ÜNİVERSİTESİ
  33. AHMET UÇAR
  34. NESİBE AKYÜREK NECMETTİN ERBAKAN ÜNİVERSİTESİ
  35. EMİNE DEMET AKBAŞ
  36. emregül ışık
  37. SARE BETÜL KAYGUSUZ İSTANBUL MEDENİYET ÜNİVERSİTESİ
  38. ZÜMRÜT KOCABEY SÜTÇÜ
  39. GÜLCAN SEYMEN
  40. MERİH BERBEROĞLU