Macroglossia associated with 271 bp deletion in exon 50 of dystrophin gene
Macroglossia is rare in patients of Duchenne muscular dystrophy (DMD), and its occurrence without any endocrinologic abnormality, seizures or an abnormal karyotype is even rarer. We describe a patient of DMD with isolated macroglossia with 271 bp deletion in exon 50 of the dystrophin gene and specul...
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| Autors principals: | , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer Medknow Publications
2011-01-01
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| Col·lecció: | Annals of Indian Academy of Neurology |
| Matèries: | |
| Accés en línia: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2011;volume=14;issue=1;spage=47;epage=49;aulast=Malhotra |
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