1.
Neurosciences. 2008; 13 (3): 305-307
in English
| IMEMR
| ID: emr-89250
ABSTRACT
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 presented with delayed motor milestones and hypotonia. The clinical features, biopsy findings, and neuroimaging abnormalities in our patient are described
Subject(s)
Humans , Male , Inheritance Patterns , Muscle Hypotonia , Muscular Dystrophies/diagnosis , Laminin , Biopsy , Magnetic Resonance Imaging , Creatine Kinase , Electromyography
2.
Indian J Pathol Microbiol
; 1984 Jul; 27(3): 169-71
Article
in English
| IMSEAR
| ID: sea-74533