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1.
Chinese Journal of Applied Clinical Pediatrics ; (24): 64-66, 2022.
Artigo em Chinês | WPRIM | ID: wpr-930372

RESUMO

A case of limb girdle muscular dystrophy type 2S (LGMD2S) caused by maternal uniparental disomy on chromosome 4 at the First Affiliated Hospital of Henan University of Chinese Medicine in March 2020 was reported.The female child, aged 9 months and 4 days, presented with developmental delay after bacterial meningitis in early infancy, decreased muscle strength in infancy and increased muscle and liver enzymes.Family genetic analysis showed that the child′s monodiploid in chromosome 4 was maternal origin, and the homozygous c. 1066T > G (p.Y356D) of TRAPPC11 gene may had pathogenic variation, which came from the child′s mother.The final diagnosis of LGMD2S was made according to the clinical manifestations and gene test results.LGMD2S is a rare autosomal recessive disease caused by the pathogenic variation of TRAPPC11 gene.Its clinical characteristics include proximal limb weakness, motor and intellectual retardation, seizures, motor disorders, elevated serum creatine kinase and muscular dystrophy like pathological changes in children.

2.
Chinese Medical Equipment Journal ; (6)2003.
Artigo em Chinês | WPRIM | ID: wpr-590046

RESUMO

The dominant position of Bundeswehr makes its field medical equipment representative in European troops.With a history more than 50 years,Bundeswehr's field medical equipment passes through 4 phases and has evolved into a complete system,which adopts backpacks,chests,vehicles and containers as the main carrier to adapt to different requirements of field medical service.Bundeswehr's field medical equipment is gifted with such tendencis as high mobility and informatization level.

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