Diagnosis of Duchenne Muscular Dystrophy Before Circumcision: A Very Early Diagnosis

S. Sarıcı, Kübra Deretarla, Lutfiye İdil Emral, C. Cerén, Hatice Ece Özütok, D. Altun, D. Sarıcı
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Abstract

Duchenne muscular dystrophy (DMD) is an X linked recessive disorder caused by a deficient or defective synthesis of dystrophine protein. Children with DMD are rarely symptomatic at birth or in early infancy, and the diagnosis is extremely difficult to establish and even it is made by chance. In this article a 5.5month-old infant in whom increases in liver function tests were detected in routine tests performed for general anesthesia and later diagnosed as Duchenne muscular dystrophy is presented. It has been emphasized that DMD, as a rare disease should be considered in etiological investigations in infants with elevations in liver function tests of any origin but with normal physical examination findings, and the utility of testing for simple biochemical markers such as creatinin kinase in establishing diagnosis before performing further detailed investigations should be kept in mind.
包皮环切术前杜氏肌萎缩症的诊断:一个非常早期的诊断
杜氏肌营养不良症(DMD)是一种由肌营养不良蛋白合成缺陷引起的X连锁隐性疾病。患有DMD的儿童在出生或婴儿期早期很少有症状,诊断非常难以确定,甚至是偶然做出的诊断。本文报道一例5.5个月大的婴儿,在全身麻醉常规检查中发现肝功能增高,后来被诊断为杜氏肌营养不良。需要强调的是,DMD作为一种罕见疾病,在对任何来源的肝功能检查升高但体格检查结果正常的婴儿进行病因学调查时应考虑到这一点,在进行进一步详细调查之前,应记住检测简单的生化标志物(如肌凝素激酶)在确定诊断方面的效用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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