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Your search keyword '"Atri S"' showing total 3 results
Start Over Author "Atri S" Journal neurology india
3 results on '"Atri S"'

1. Nemaline rod myopathy: A rare form of myopathy

Author

Sharma, M., Gulati, S., Atri, S., Seth, R., Kalra, V., Das, T., and Sarkar, C.

Subjects
Diagnosis, Observations, Case studies, Pediatric diseases -- Case studies -- Diagnosis, Biopsy -- Observations -- Case studies, Genetic disorders -- Case studies -- Diagnosis, Muscular diseases -- Case studies -- Diagnosis, Children -- Diseases, Muscle diseases -- Case studies -- Diagnosis
Published
2007

3. Congenital fiber type disproportion: a rare type of congenital myopathy: a report of four cases.

Author

Sharma MC, Ralte AM, Atri SK, Gulati S, Kalra V, and Sarkar C

Subjects
Adolescent, Biopsy, Child, Child, Preschool, Diagnosis, Differential, Female, Histocytochemistry methods, Humans, Male, Muscle, Skeletal metabolism, Myopathies, Structural, Congenital metabolism, Staining and Labeling, Muscle, Skeletal pathology, Myopathies, Structural, Congenital pathology
Abstract

Congenital fiber type disproportion is a rare type of congenital myopathy which presents as hypotonia, delayed motor milestones and dysmorphic facies. During the past 2 years we received 449 muscle biopsies, of which 4 cases were diagnosed as congenital fiber type disproportion (CFTD). In addition to CFTD, one case also had centronuclear features. Three of them were females and one was a male child. Although rare, it should be considered in the differential diagnosis of childhood muscle diseases. Histochemical staining is necessary for the diagnosis of this entity.

Published
2004

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