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akaturk Akademik ölçüm

Makale detayı · 2025

A Little Known but Very Common Phenotype in Patients With Severe Congenital Neutropenia Due to HAX1 Deficiency: Premature Ovarian Insufficiency

Pediatric Blood & Cancer

YÖKSİS OpenAlex Açık erişim · hybrid SJR Q1 JCR Q2 Atıf 2 Yüzdelik 80.4% FWCI 1.57
Yıl
2025
ISSN
1545-5009
Tür
article

Veri kaynağı ayrımı

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

Özet

İngilizce (OpenAlex)

BACKGROUND: Autosomal recessive severe congenital neutropenia (SCN) has been associated with homozygous variants in the HAX1 gene. The aim of this cross-sectional study was to evaluate the gonadal function and pubertal development in pediatric patients with SCN due to HAX1 gene variant (HAX1-SCN). METHODS: Forty-five patients, including 24 females (median age 11.3 [1.5-31] years, 13 pubertal, 11 prepubertal), and 21 males (median age 9.5 (3-18.8) years, 7 pubertal, 14 prepubertal), followed in seven centers, were included. POI is defined as a menstrual disturbance with increased follicle-stimulating hormone (FSH) and low anti-Mullerian hormone (AMH). We classified prepubertal female patients as impending POI when they had low AMH and high FSH values, indicating impaired ovarian function. RESULTS: A homozygous single nucleotide insertion (position 130-131insA) leading to a premature stop codon; p.Trp44*(c.132G>A) variant in HAX1 gene was detected in 42 (93.3%) affected individuals. Other homozygous variants were p.Arg86*(c.256C>T) and p.Glu60Aspfs*25(c.180delA). We detected elevated serum FSH levels in 10/11 (90.9%) of prepubertal female patients, supporting the diagnosis of impending POI, and in 12/13 (92.3%) of pubertal female patients, classifying them as POI. All female patients had low AMH levels. Male patients did not exhibit gonadal insufficiency. CONCLUSIONS: This is the first and largest case series covering early childhood to evaluate patients with HAX1-SCN for gonadal function. It has been observed that pubertal females develop POI, prepubertal females are at increased risk for gonadal failure, and male patients are not affected. Our results suggest that HAX1 has an important role in ovarian maturation and/or function.

Konular

  • Blood disorders and treatments
  • Platelet Disorders and Treatments
  • Blood groups and transfusion

Birincil konu Blood disorders and treatments

Yazarlar

  1. DENİZ ÖZALP KIZILAY
  2. DENİZ YILMAZ KARAPINAR
  3. NİHAL KARADAŞ
  4. MURAT KARAOĞLAN
  5. SİNAN AKBAYRAM
  6. RUHSAR DAMLA GÖKŞEN
  7. AYŞE GADASHOVA
  8. SERPİL ALBAYRAK
  9. ESRA PEKPAK ŞAHİNOĞLU
  10. ZERRİN ORBAK
  11. ZAFER BIÇAKÇI
  12. LEYLA AKIN
  13. CANAN ALBAYRAK
  14. CANSU KOÇ ÇALIŞGAN
  15. AYŞEGÜL ÜNÜVAR İSTANBUL ÜNİVERSİTESİ
  16. AHMET ANIK
  17. YUSUF ZİYA ARAL
  18. EMİNE AYÇA CİMBEK
  19. AYŞENUR BAHADIR
  20. CEM METE
  21. SAMİM ÖZEN