نتایج جستجو برای: ullrich congenital muscular dystrophy

تعداد نتایج: 169567  

2014
Satoru Noguchi Megumu Ogawa Genri Kawahara May Christine Malicdan Ichizo Nishino

Ullrich congenital muscular dystrophy (UCMD) is an inherited muscle disorder characterized clinically by muscle weakness, distal joint hyperlaxity, and proximal joint contractures. Sporadic and recessive mutations in the three collagen VI genes, COL6A1, COL6A2, and COL6A3, are reported to be causative. In the sporadic forms, a heterozygous point mutation causing glycine substitution in the trip...

Journal: :Neurosciences 2008
Amna Al-Futaisi Almundher Al-Maawali Raghad Abdwani Vasudev T Rao Hashim Javad Roshan Koul

Merosin-deficient congenital muscular dystrophy is an autosomal recessive disease that can manifest differently in different ethnic groups. This often presents as a floppy infant, and normal mental development. The creatine kinase is usually elevated with white matter abnormalities on brain imaging. In this report, we describe an infant with Merosin-deficient congenital muscular dystrophy who p...

Journal: :Human molecular genetics 2005
Naomi L Baker Matthias Mörgelin Rachel Peat Nathalie Goemans Kathryn N North John F Bateman Shireen R Lamandé

Mutations in the three collagen VI genes COL6A1, COL6A2 and COL6A3 cause Bethlem myopathy and Ullrich congenital muscular dystrophy (UCMD). UCMD, a severe disorder characterized by congenital muscle weakness, proximal joint contractures and marked distal joint hyperextensibility, has been considered a recessive condition, and homozygous or compound heterozygous mutations have been defined in CO...

Journal: :American journal of human genetics 2002
Ercan Demir Patrizia Sabatelli Valérie Allamand Ana Ferreiro Behzad Moghadaszadeh Mohamed Makrelouf Haluk Topaloglu Bernard Echenne Luciano Merlini Pascale Guicheney

Ullrich congenital muscular dystrophy (UCMD) is an autosomal recessive disorder characterized by generalized muscular weakness, contractures of multiple joints, and distal hyperextensibility. Homozygous and compound heterozygous mutations of COL6A2 on chromosome 21q22 have recently been shown to cause UCMD. We performed a genomewide screening with microsatellite markers in a consanguineous fami...

Journal: :Trends in pharmacological sciences 2003
Enca Martin-Rendon Derek J Blake

Glycosylation is the most frequent modification of proteins and is important for many ligand-receptor interactions. Recently, defects in protein glycosylation have been linked to several forms of congenital muscular dystrophy that are frequently associated with brain abnormalities. Muscle-eye-brain disease and Walker-Warburg syndrome are caused by mutations in enzymes involved in O-mannosylatio...

2014
Silvia Toni Riccardo Morandi Marcello Busacchi Lucia Tardini Luciano Merlini Nino Carlo Battistini Massimo Pellegrini

Collagen VI mutations lead to disabling myopathies like Bethlem myopathy (BM) and Ullrich congenital muscular dystrophy (UCMD). We have investigated the nutritional and metabolic status of one UCMD and seven BM patients (five female, three male, mean age 31 ± 9 years) in order to find a potential metabolic target for nutritional intervention. For this study, we used standard anthropometric tool...

Journal: :AJNR. American journal of neuroradiology 1994
N Aida A Yagishita K Takada Y Katsumata

PURPOSE To determine the MR appearance of cerebellar abnormalities in Fukuyama congenital muscular dystrophy. METHODS We reviewed brain MR images of 25 patients with Fukuyama congenital muscular dystrophy and examined the autopsy specimens of a 23-month-old girl with the disease to determine the pathologic nature of the MR findings. RESULTS MR studies revealed two characteristic cerebellar ...

Journal: :American journal of human genetics 2011
Satomi Mitsuhashi Aya Ohkuma Beril Talim Minako Karahashi Tomoko Koumura Chieko Aoyama Mana Kurihara Ros Quinlivan Caroline Sewry Hiroaki Mitsuhashi Kanako Goto Burcu Koksal Gulsev Kale Kazutaka Ikeda Ryo Taguchi Satoru Noguchi Yukiko K Hayashi Ikuya Nonaka Roger B Sher Hiroyuki Sugimoto Yasuhito Nakagawa Gregory A Cox Haluk Topaloglu Ichizo Nishino

Congenital muscular dystrophy is a heterogeneous group of inherited muscle diseases characterized clinically by muscle weakness and hypotonia in early infancy. A number of genes harboring causative mutations have been identified, but several cases of congenital muscular dystrophy remain molecularly unresolved. We examined 15 individuals with a congenital muscular dystrophy characterized by earl...

Journal: :AJNR. American journal of neuroradiology 1999
P A Caro M Scavina E Hoffman E Pegoraro H G Marks

BACKGROUND AND PURPOSE Our purpose was to determine the brain MR imaging characteristics of merosin-deficient congenital muscular dystrophy in children. METHODS We reviewed the MR imaging findings of the brain in three children with known merosin-deficient congenital muscular dystrophy to determine the presence of any cerebral or cerebellar abnormalities of development or abnormalities of the...

2014
Francesca Gattazzo Sibilla Molon Valeria Morbidoni Paola Braghetta Bert Blaauw Anna Urciuolo Paolo Bonaldo

Mutations of genes encoding for collagen VI cause various muscle diseases in humans, including Bethlem myopathy and Ullrich congenital muscular dystrophy. Collagen VI null (Col6a1 (-/-)) mice are affected by a myopathic phenotype with mitochondrial dysfunction, spontaneous apoptosis of muscle fibers, and defective autophagy. Moreover, Col6a1 (-/-) mice display impaired muscle regeneration and d...

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