Analysis of duplications versus deletions in the dystrophin gene in Serbian cohort with dystrophinopathies

Author:

Maksic Jasmina1,Dobricic Valerija2,Rasulic Lukas3,Maksimovic Nela4,Branakovic Marija4,Milic-Rasic Vedrana5,Rakocevic-Stojanovic Vidosava6,Novakovic Ivana4ORCID

Affiliation:

1. University of Belgrade, Faculty for Special Education and Rehabilitation, Belgrade, Serbia

2. Clinical Center of Serbia, Neurology Clinic, Belgrade, Serbia

3. University of Belgrade, Faculty of Medicine, Belgrade, Serbia + Clinical Center of Serbia, Clinic for Neurosurgery, Belgrade, Serbia

4. University of Belgrade, Faculty of Medicine, Belgrade, Serbia

5. University of Belgrade, Faculty of Medicine, Belgrade, Serbia + Clinic for Neurology and Psychiatry for Child and Youth, Belgrade, Serbia

6. Clinical Center of Serbia, Neurology Clinic, Belgrade, Serbia + University of Belgrade, Faculty of Medicine, Belgrade, Serbia

Abstract

Background/Aim. Duchenne muscular dystrophy (DMD) and its allelic form Becker muscular dystrophy (BMD) are X-linked diseases that affect males, characterized by progressive muscle and cardiopulmonary weakness, especially in DMD as a severe form of the disease. They result from mutations in the dystrophin gene, and the most common changes are large intragenic deletions and duplications (80%). One third of patients have de novo mutation and 2/3 of the mothers are estimated as carriers. The aim of the study was to analyze the frequency of duplications versus deletions in the dystrophin gene in patients with dystrophinopathies, as well as to analyze the phenotypic effect of large mutations obtained and to determine the carrier status of female relatives in probands with duplications. Methods. We examined 22 DMD and 35 BMD unrelated patients and 6 female relatives of the probands where duplications were found. We used polymerase chain reaction (PCR) and multiplex ligation-dependent probe amplification (MLPA) methods, according to the protocol, to detect or confirm mutations in probands and female carriers. Results. In probands, there were 34 (59.6%) large deletions (mostly affected exons 44?60) and 6 (10.5%) large duplications in 4 DMD and 2 BMD patients. Also, duplications were found in 3 out of 4 (75%) tested mothers. The distribution of duplications was heterogeneous, affecting N-terminal and central rod domain, and included more exons, except for one DMD patient who had duplication of exon 2. An exception from the Monaco rule was present in 9.5% of DMD and 15.8% of BMD probands, i.e. in 12.5% of DMD/BMD cases. Conclusion. In 57 DMD/BMD probands, we found 59.6% of large deletions and 10.5% of large duplications. The most affected region of the DMD gene was the central rod domain. An exception to Monaco''s rule was present in 12.5% of DMD/BMD cases. Three out of 4 examined proband''s mothers were confirmed as carriers.

Funder

Ministry of Education, Science and Technological Development of the Republic of Serbia

Publisher

National Library of Serbia

Subject

Pharmacology (medical),General Medicine

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