Alleviation of masticatory disturbance with an occlusal splint in a Duchenne muscular dystrophy patient
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چکیده
منابع مشابه
Duchenne muscular dystrophy An overview of Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) affects approximately 1 in 3,500 live male births [1]. It is caused by a large variety of mutations in the dystrophin gene. Because of these mutations, the body can no longer make dystrophin which is a protein important for stabilisation of the muscle cell during a contraction. Without dystrophin, muscle cells are damaged and slowly replaced by fat and scar tis...
متن کاملP164: Adeno-Associated Viral Vectors in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (BMD) is an inherited X-link disease. The incidence of this muscle-wasting disease is 1:5000 male live births. Mutation in the gene coding for dystrophin is the main cause of BMD. Most cases of this disease succumb to respiratory and cardiac failure in 3rd to 4th decades. The slow progression of BMD and recent achievement of gene therapies make it as an appropriate c...
متن کاملDetection of the Duplication in Exons 56-63 of Duchenne Muscular Dystrophy Patients with MLPA
Background Duchenne Muscular Dystrophy (DMD) is a deadly X-linked recessive disorder. This genetic disorder affects 1 among 3,500-5,000 males in the world. The majority of the patients are male, due to the type of inheritance. It affects most of the skeletal, the respiratory, and cardiac muscles, causing these vital organs to contract and eventually mortality.<br...
متن کاملDisturbed sleep in a patient with Duchenne muscular dystrophy.
173 A 17-year-old white male with Duchenne muscular dystrophy presented to the pediatric pulmonary clinic for a follow-up evaluation after being hospitalized for pneumonia. During the hospital stay he was noted to have nocturnal desaturation intermittently during sleep. The patient has been wheelchair bound since age 12 years. His father’s two current concerns include the patient’s difficulty s...
متن کاملTracheocoele in a Duchenne muscular dystrophy patient. Case report.
Tracheocoele, a congenital or acquired lesion, is rarely detected radiologically and even more rarely diagnosed clinically. This tracheal lesion is characterised by the presence of a single cystic lesion filled with air or a mixture of liquid and air, of extremely variable size, occurring in almost all cases, in a locus minoris resistentiae situated in the right posterolateral portion of the tr...
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ژورنال
عنوان ژورنال: Special Care in Dentistry
سال: 2021
ISSN: 0275-1879,1754-4505
DOI: 10.1111/scd.12594