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Congenital muscular dystrophy with characteristic radiological findings similar to those with Fukuyama congenital muscular dystrophy, 10/2004
Fukuyama congenital muscular dystrophy (FCMD) is the most common congenital muscular dystrophy in Japan and there are isolated reports of non-Japanese patients... 
Neurology | Fukuyama congenital muscular dystrophy, congenital muscular dystrophy ni04166
Journal
Journal Article
Brain and Development, ISSN 0387-7604, 01/2019, Volume 41, Issue 1, pp. 43 - 49
The leading cause of death in patients with Fukuyama congenital muscular dystrophy (FCMD) is congestive heart failure or respiratory dysfunction, which is same... 
Creatinine | Fanconi syndrome | ACE inhibitor | Fukuyama congenital muscular dystrophy | Renal dysfunction | Cystatin C | RISK | KIDNEY | CLINICAL NEUROLOGY | Urine | Medical colleges | Divalproex | Cardiac patients | Epilepsy | Analysis | Medical genetics | Valproic acid | Health aspects | Muscular dystrophy | Natriuretic peptides
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 12/2010, Volume 25, Issue 12, pp. 1559 - 1581
Journal Article
Brain & Development, ISSN 0387-7604, 2017, Volume 39, Issue 7, pp. 613 - 616
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 10/2018, Volume 28, Issue 10, pp. 885 - 893
Fukuyama congenital muscular dystrophy (FCMD) is the second most common form of muscular dystrophy in the Japanese population and is caused by mutations in the... 
Patient registry | Japan Muscular Dystrophy Association (JMDA) | Natural history | Fukuyama congenital muscular dystrophy | FKTN | CARDIAC INVOLVEMENT | NEUROSCIENCES | CLINICAL NEUROLOGY | Heart | Medicine, Experimental | Medical research | Epidemiology | Epilepsy | Muscular dystrophy
Journal Article
Journal Article
PAKISTAN JOURNAL OF MEDICAL SCIENCES, ISSN 1682-024X, 04/2012, Volume 28, Issue 3, pp. 519 - 521
Muscular dystrophy is an inherited group of disorders that affects skeletal and many other systems. It is transferred to the next generations with autosomal... 
Fukuyama syndrome | MEDICINE, GENERAL & INTERNAL | Hypotonia | Autosomal recessive disorder | Convulsion
Journal Article
Neurology and Clinical Neuroscience, ISSN 2049-4173, 07/2018, Volume 6, Issue 4, pp. 115 - 116
We report the case of a 16‐year‐old boy in whom Fukuyama congenital muscular dystrophy (FCMD) had been genetically diagnosed. He required mechanical... 
respiratory failure | bronchus obstruction | Fukuyama congenital muscular dystrophy | scoliosis | positive end‐expiratory pressure
Journal Article
AMERICAN JOURNAL OF HUMAN GENETICS, ISSN 0002-9297, 12/2001, Volume 69, Issue 6, pp. 1198 - 1209
The congenital muscular dystrophies (CMD) are a heterogeneous group of autosomal recessive disorders presenting in infancy with muscle weakness, contractures,... 
ENMC SPONSORED WORKSHOP | LOCALIZATION | FUKUYAMA-TYPE | MENTAL-RETARDATION | BIOSYNTHESIS | FAMILIES | GENETICS & HEREDITY | MUSCLE | EXTRACELLULAR-MATRIX | NETHERLANDS | MEROSIN DEFICIENCY
Journal Article
Brain & Development, ISSN 0387-7604, 2015, Volume 37, Issue 9, pp. 880 - 886
Abstract Purpose Fukuyama congenital muscular dystrophy (FCMD) is a congenital muscular dystrophy rarely reported outside Japan. Here, we report three patients... 
Neurology | Founder mutation | Haplotype analysis | Fukuyama congenital muscular dystrophy | 3-kb insertion | FKTN | DEFECTIVE GLYCOSYLATION | INVOLVEMENT | WALKER-WARBURG-SYNDROME | FUKUTIN | PHENOTYPE | DYSTROGLYCAN | CLINICAL NEUROLOGY | GENE | RETROTRANSPOSAL INSERTION | DISEASE | Genetic aspects | Muscular dystrophy
Journal Article