Component of conserved oligomeric Golgi complex 7 deficiency (Q103661): Difference between revisions
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CID11:ID_808184224 | |||||||||||||||
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dki-india-ID_808184224 | |||||||||||||||
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16 August 2026
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Latest revision as of 09:25, 17 August 2026
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIe is characterised by dysmorphism, skeletal dysplasia, hypotonia, hepatosplenomegaly, jaundice, cardiac insufficiency, recurrent infections and epilepsy. To date, it has been described in two infants, both of whom died within the first three months of life. The syndrome is caused by a mutation in the gene encoding COG-7 (chromosome 16), a subunit of the oligomeric Golgi complex.
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| default for all languages | ID_808184224 |
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| English | Component of conserved oligomeric Golgi complex 7 deficiency |
The CDG (Congenital Disorders of Glycosylation) syndromes are a group of autosomal recessive disorders affecting glycoprotein synthesis. CDG syndrome type IIe is characterised by dysmorphism, skeletal dysplasia, hypotonia, hepatosplenomegaly, jaundice, cardiac insufficiency, recurrent infections and epilepsy. To date, it has been described in two infants, both of whom died within the first three months of life. The syndrome is caused by a mutation in the gene encoding COG-7 (chromosome 16), a subunit of the oligomeric Golgi complex. |
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CID11:ID_808184224
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dki-india-ID_808184224
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Concluído
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16 August 2026
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