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Nascer e Crescer

versión impresa ISSN 0872-0754

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BANDEIRA, Anabela et al. Genes, crianças e pediatras. Nascer e Crescer [online]. 2011, vol.20, n.2, pp.101-103. ISSN 0872-0754.

A 14 month-old boy presented with failure to thrive and severe mental and motor development delay. On physical examination he presented with severe axial hypotonia and dysmorphic syndrome: peculiar facies with small eyes, micrognathia, raised intermamilar distance. He also had multissistemic involvement with nephritic proteinuria, hypertrophy cardiomiopathy with peri­cardial effusion, raised transaminases, functional deficit of coagulation proteins and unspecific changes of retinal pigmentation. This case illustrates the typical presentation of congenital disorder of glycosilation (CDG) type Ia.

Palabras clave : congenital disorder of glycosilation; glycosylated transferring.

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