A Case of Hemoglobin Lepore Syndrome
スポンサーリンク
概要
- 論文の詳細を見る
A 4-year-old boy with microcytic anemia without iron deficiency is reported. Isoelectrofocusing analysis showed an abnormal hemoglobin (Hb) band likely to be Hb Lepore syndrome, one of the thalassemia-like disorders. He was then diagnosed with Hb Lepore (Washington-Boston type) syndrome by specific gap PCR. While patients with a mild type of thalassemia or thalassemia-like syndrome should have normal life prognoses, definite diagnosis is important because of the problems of hereditary counseling.
- 特定非営利活動法人 日本小児血液・がん学会の論文
特定非営利活動法人 日本小児血液・がん学会 | 論文
- The Parent's Emotional Adaptation to the Children's Malignant Disease
- Side Effect of Cranial Radiation in Childhood Acute Leukemia
- Red Blood Cell Volume Distribution Width in Normal Children and in the Patients with Various Kinds of Hematological Disorders.
- Effective Conditioning of Donors for Granulocyte Transfusions with Recombinant Human Granulocyte Colony-Stimulating Factor.
- Two Infant Girls of CNS Leukemia with Chronic Subdural Hematoma