İçeriğe geç
akaturk Akademik ölçüm

Makale detayı · 2023

Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation

HEMOGLOBIN

YÖKSİS OpenAlex SJR Q3 JCR Q4 Atıf 1 Yüzdelik 50.5% FWCI 0.16
Yıl
2023
ISSN
0363-0269
Tür
article

Veri kaynağı ayrımı

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

Özet

İngilizce (OpenAlex)

Hemoglobin (Hb) Hammersmith, formed by serine substitution for phenylalanine at residue 42 in the beta-globin chain, is a very rare variant of unstable hemoglobin with low oxygen affinity. For patients with hemoglobinopathies, it is well-established that hematopoietic stem cell transplantation provides a complete cure, but the literature on its role for those with Hb Hammersmith is limited. A seven-month-old girl who was examined for anemia and splenomegaly was followed up for congenital hemolytic anemia. The patient with visible cyanosis of the lips and whose p50 was low in blood gas was diagnosed with Hb Hammersmith through the DNA sequence analysis. During the follow-up, frequent blood transfusions had to be given due to anemia aggravated by infections. Following a successful hematopoietic stem cell transplant from an HLA-matched sibling, the patient completely recovered from Hb Hammersmith. The case is presented because of its rarity.

Konular

  • Hemoglobinopathies and Related Disorders
  • Blood groups and transfusion
  • Erythrocyte Function and Pathophysiology

Birincil konu Hemoglobinopathies and Related Disorders

Yazarlar

  1. AYŞEN TÜREDİ YILDIRIM MANİSA CELÂL BAYAR ÜNİVERSİTESİ
  2. HÜSEYİN GÜLEN
  3. HÜLYA TÜRKMEN
  4. GÜLCİHAN ÖZEK EGE ÜNİVERSİTESİ
  5. YEŞİM OYMAK
  6. MEHMET BURAK DURMAZ
  7. EMİN KARACA EGE ÜNİVERSİTESİ