Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patients
| Autor: | Xiru Wu, Hui Jiao, Hui Xiong, Tatsushi Toda, Kazuhiro Kobayashi, Jiangxi Xiao, Shuo Wang, Haipo Yang |
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| Rok vydání: | 2014 |
| Předmět: |
Male
Pathology medicine.medical_specialty Compound heterozygosity Exon Developmental Neuroscience Asian People Fukuyama congenital muscular dystrophy Medicine Humans Child Muscle Skeletal 3' Untranslated Regions business.industry Haplotype Muscle weakness Brain Infant Membrane Proteins Walker-Warburg Syndrome General Medicine medicine.disease Fukutin Founder Effect Child Preschool Pediatrics Perinatology and Child Health Mutation Congenital muscular dystrophy Female Neurology (clinical) medicine.symptom business Micropolygyria |
| Zdroj: | Braindevelopment. 37(9) |
| ISSN: | 1872-7131 |
| Popis: | Purpose Fukuyama congenital muscular dystrophy (FCMD) is a congenital muscular dystrophy rarely reported outside Japan. Here, we report three patients with Fukuyama congenital muscular dystrophy (FCMD) in China who shared a similar clinical phenotype and 3-kb insertion in the FKTN 3′ untranslated region. Methods Immunofluorescence staining was undertaken on muscle biopsies from three patients using alpha dystroglycan antibody (IIH6). Genomic DNA from patients and parents was extracted from peripheral blood leukocytes. Polymerase chain reaction and DNA sequencing were employed to analyze the exons and surrounding intron sequences of the fukutin ( FKTN ) gene to detect mutations. Haplotype analysis was also performed on each patient and their parents. Results All patients had delayed mental and motor development, febrile convulsions, muscle weakness, and moderate to significant raised levels of serum creatine kinase (7000–11,160 U/L, 25–60 × normal). Brain MRI scans showed micropolygyria and extensive dysplasia in the white matter and brainstem. Electromyography revealed myopathic changes. Muscle immunofluorescence studies demonstrated reduced IIH6 staining. Genetic testing showed compound heterozygous mutations of FKTN . Cases 1 and 2 had a c.139C>T (p.Arg47 ∗ ) heterozygous mutation. Case 3 had a c.346C>T (p.Gln116 ∗ ) heterozygous mutation. Conclusion All patients had a heterozygous 3-kb insertion in the FKTN 3′ untranslated region. Haplotype analyses suggested that these patients had the same haplotype as Japanese patients. |
| Databáze: | OpenAIRE |
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