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Dyskeratosis Congenita

机译:先天性角化病

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Importance: Dyskeratosis congenita is a rare disorder that often leads to early death owing to a variety of complications and associated disorders.? Early diagnosis and intervention is important in care for patients affected by this disease. Observations: We describe a patient with dyskeratosis congenita (DC) in a child. Our patient had a 3-year history of transaminitis that was felt to be the result of biopsy proven progressive fibrosis of the liver beginning at age 3. He was referred to the dermatology department because of a chronic, evolving eruption with the hope of establishing a unifying diagnosis.? Further examination revealed dystrophic nails, numerous dental caries, and blepharitis.? Chromosomal analysis on leukocytes showed significant telomere shortening consistent with DC. Conclusions and Relevance: Early recognition and long term care is important in patients with DC because of their propensity to develop malignancy, hematologic abnormalities, and infection.? Better understanding of this disease may lead to insights into other disorders associated with abnormal telomere maintenance.
机译:重要性:先天性角化病是一种罕见的疾病,由于各种并发症和相关疾病,通常会导致早期死亡。早期诊断和干预对于照顾受该病影响的患者非常重要。观察结果:我们描述了一名儿童先天性角化病(DC)的患者。我们的患者有3年的转氨炎病史,被认为是从3岁开始活检证实的肝脏进行性纤维化的结果。由于慢性不断发展的爆发,他被转诊至皮肤科,希望建立一个统一诊断。进一步检查发现营养不良的指甲,大量龋齿和睑缘炎。对白细胞的染色体分析表明端粒明显缩短,与DC一致。结论与相关性:由于DC患者倾向于发生恶性肿瘤,血液学异常和感染,因此对其进行早期识别和长期护理很重要。更好地了解这种疾病可能会导致洞悉端粒维持异常相关的其他疾病。

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