CASE REPORT |
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Year : 2022 | Volume
: 5
| Issue : 3 | Page : 192-193 |
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Tourette syndrome in Duchenne muscular dystrophy: A rare case
Nikhil Jadhav, Agrata Sharma, Nirendra Rai, Ayush Dubey, Abhijeet K Kohat
Department of Neurology, All India Institute of Medical Sciences, Bhopal, Madhya Pradesh, India
Correspondence Address:
Dr. Abhijeet K Kohat Department of Neurology, All India Institute of Medical Sciences, Bhopal - 462 020, Madhya Pradesh India
 Source of Support: None, Conflict of Interest: None
DOI: 10.4103/AOMD.AOMD_66_21
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Duchenne Muscular Dystrophy (DMD) is an X-linked recessive muscular dystrophy that presents in the first decade of life. Neurodevelopmental disorders are increasingly recognized features in DMD including autistic spectrum disorder, attention-deficit– hyperactivity disorder, and obsessive-compulsive disorder. The presence of Gilles De La Tourette Syndrome (GTS) in DMD patients is extremely rare. GTS in DMD patients supports the hypothesis that disruption of different dystrophin isoforms may play a role in brain development and function. |
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