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Prolonged thrombocytopenia in a neonate with Noonan syndrome: a case report

机译:延长血小板减少血小阴蛋白在Neonanate中Noonan综合征:案例报告

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摘要

We report a case of a Chinese neonate who was diagnosed with Noonan syndrome and had persistent, self-limited thrombocytopenia. The neonate was admitted to the Neonatology Department 20 minutes after birth because of respiratory distress. From birth until 2 months of age, platelet values fluctuated between approximately 6 and 30 × 109/L. There was no intracranial hemorrhage. However, the child had a transient hypocalcemic seizure and fever. We excluded thrombocytopenia caused by perinatal asphyxia, immune thrombocytopenia, fetomaternal alloimmune thrombocytopenia, juvenile myelomonocytic leukemia, and chromosome 13, 18, and 21 trisomy syndromes. Despite treatment with anti-infective agents and transfusion of platelets and immunoglobulin, the platelet count did not return to the normal range. Genetic testing confirmed a PTPN11 gene mutation, which led to the diagnosis of Noonan syndrome. At 3 months of age, the platelet count gradually increased without intervention and returned to the normal range by 6 months. We speculate that the thrombocytopenia in this case was closely related to Noonan syndrome.
机译:我们举报了一个被诊断患有Noonan综合征的中国新生儿的案例,并且具有持续的自动限制血小板减少症。由于呼吸窘迫,出生后20分钟内接纳了新生儿。从出生到2个月的年龄,血小板值波动在大约6和30×109 /升之间。没有颅内出血。然而,孩子患有短暂的低钙糖癫痫发烧和发烧。我们排除了由围产期窒息,免疫血小板减少症,胎儿血小毒症血小板减少症,青少年骨髓细胞白血病和染色体13,18和21个三胞综合征引起的血小阴十尼血症。尽管用抗感染剂治疗和血小板输血和免疫球蛋白,但血小板计数没有恢复到正常范围。基因检测证实了一种PTPN11基因突变,导致了非洲综合征的诊断。在3个月的年龄时,血小板计数逐渐增加而无需干预,并恢复到正常范围6个月。我们推测,这种情况下的血小板减少症与日死综合征密切相关。

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