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Makale detayı · 2021 · article

Clinical and Hormonal Profiles Correlate With Molecular Characteristics in Patients With 11β-Hydroxylase Deficiency

Dergi The Endocrine Society ISSN kaydı başka bir dergiye işaret ediyor; ad YÖKSİS kaydından.
ISSN0021-972X
YÖKSİS OpenAlex Açık erişim · bronze
Yıl2021
Atıf43OpenAlex
Yüzdelik%89,1
FWCI2,241,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıThe Endocrine Society
  • Katalog eşleşmesi (ISSN)Journal of Clinical Endocrinology and Metabolism
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

BACKGROUND: Given the rarity of 11β-hydroxylase deficiency (11βOHD), there is a paucity of data about the differences in clinical and biochemical characteristics of classic (C-11βOHD) and nonclassic 11βOHD (NC-11βOHD). OBJECTIVE: To characterize a multicenter pediatric cohort with 11βOHD. METHOD: The clinical and biochemical characteristics were retrospectively retrieved. CYP11B1 gene sequencing was performed. Seventeen plasma steroids were quantified by liquid chromatography-mass spectrometry and compared to that of controls. RESULTS: 102 patients (C-11βOHD, n = 92; NC-11βOHD, n = 10) from 76 families (46,XX; n = 53) had biallelic CYP11B1 mutations (novel 9 out of 30). Five 46,XX patients (10%) were raised as males. Nineteen patients (19%) had initially been misdiagnosed with 21-hydroxylase deficiency. Female adult height was 152 cm [-1.85 SD score (SDS)] and male 160.4 cm (-2.56 SDS).None of the NC-11βOHD girls had ambiguous genitalia (C-11βOHD 100%), and none of the NC-11βOHD patients were hypertensive (C-11βOHD 50%). Compared to NC-11βOHD, C-11βOHD patients were diagnosed earlier (1.33 vs 6.9 years; P < 0.0001), had higher bone age-to-chronological age (P = 0.04) and lower adult height (-2.46 vs -1.32 SDS; P = 0.05). The concentrations of 11-oxygenated androgens and 21-deoxycortisol were low in all patients. The baseline ACTH and stimulated cortisol were normal in NC-11βOHD. Baseline cortisol; cortisone; 11-deoxycortisol; 11-deoxycorticosterone and corticosterone concentrations; and 11-deoxycortisol/cortisol, 11-deoxycorticosterone/cortisol, and androstenedione/cortisol ratios were higher in C-11βOHD than NC-11βOHD patients (P < 0.05). The 11-deoxycortisol/cortisol ratio >2.2, <1.5, and <0.1 had 100% specificity to segregate C-11βOHD, NC-11βOHD, and control groups. CONCLUSION: NC-11βOHD can escape from clinical attention due to relatively mild clinical presentation. However, steroid profiles enable the diagnosis, differential diagnosis, and subtyping of 11βOHD.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

43atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 22 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  2. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  3. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  4. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  5. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  6. 2022 Steroid Hormone Profiles and Molecular Diagnostic Tools in Pediatric Patients With non-CAH Primary Adrenal InsufficiencyAtıf 15 · OpenAlex
  7. 2025 Primary adrenal insufficiency in patients with CPOX gene mutationsAtıf 6 · OpenAlex
  8. 2023 Case Report: A Novel Mutation Leading to 11-β hydroxylase Deficiency in a Female PatientAtıf 3 · OpenAlex
  9. 2023 Case Report: A Novel Mutation Leading to 11-β Hydroxylase Deficiency in a Female PatientAtıf 3 · OpenAlex
  10. 2022 A Novel Mutation Leading to 11- hydroxylase Deficiency in a Female PatientAtıf 3 · OpenAlex

Yazarlar

7
  1. MELEK YILDIZ 1
  2. FİRDEVS BAŞ 2
  3. FATMA DURSUN SAĞLIK BİLİMLERİ ÜNİVERSİTESİ 3
  4. ZEHRA YAVAŞ ABALI 4
  5. FATMA FEYZA DARENDELİLER 5
  6. TÜLAY GÜRAN 6
  7. ABDULLAH BEREKET MARMARA ÜNİVERSİTESİ 7