Laboratory of Molecular and Cellular Hematology, LR16IPT07, Pasteur Institute of Tunis, University of Tunis El Manar.
Molecular Biology Cell and Biotechnology Department, Higher Institute of Biotechnology of Monastir, University of Monastir, Monastir, Tunisia.
J Pediatr Hematol Oncol. 2021 Nov 1;43(8):e1055-e1058. doi: 10.1097/MPH.0000000000002096.
Several causes are known to be at the origin of neonatal cyanosis among them methemoglobinemia is by inheritance of an hemoglobin (Hb) M variant. This is a rare condition never been reported in Tunisia so far. Here, we report a Tunisian newborn with refractory cyanosis since birth. As cardiac and respiratory diseases were ruled out, methemoglobinemia was suspected. Hematological parameters, concentration of methemoglobin, capillary electrophoresis, and amplification sequencing of the HBB gene were performed. Computational analysis was achieved by different in silico tools to investigate the mutation effect. The diagnosis was established by a raised MetHb, confirmed by the presence HbM-Saskatoon [Beta63 (E7) His>Tyr] by capillary electrophoresis and molecular analysis. The identified mutation occurred as a de novo mutation. In silico analysis confirmed the pathogenicity of the mutation. To our knowledge, this is the first time that this mutation has been reported in the Tunisian population. In view of its low incidence rate, clinicians might misdiagnose cyanosis caused by HbM, which can lead to inappropriate treatment and clinical complications. An up-to-date literature review of HbM disease is presented in this study.
已知有几个原因会导致新生儿出现发绀,其中高铁血红蛋白血症是由血红蛋白 (Hb) M 变体遗传引起的。这种情况非常罕见,迄今为止在突尼斯从未有过报道。在这里,我们报告了一名突尼斯新生儿自出生以来就出现难治性发绀。由于排除了心脏和呼吸系统疾病,怀疑是高铁血红蛋白血症。进行了血液学参数、高铁血红蛋白浓度、毛细管电泳和 HBB 基因的扩增测序。通过不同的计算工具进行计算分析,以研究突变的影响。通过毛细管电泳和分子分析证实存在 HbM-Saskatoon [Beta63 (E7) His>Tyr],升高的 MetHb 确诊了诊断。该突变是一个新生突变。计算分析证实了突变的致病性。据我们所知,这是该突变首次在突尼斯人群中报道。鉴于其发病率低,临床医生可能会误诊由 HbM 引起的发绀,这可能导致不适当的治疗和临床并发症。本研究还对 HbM 疾病的最新文献进行了综述。