Component of conserved oligomeric Golgi complex 7 deficiency (Q103661): Difference between revisions
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As síndromes CDG (distúrbios congênitos de glicosilação) são um grupo de doenças autossômicas recessivas que afetam a síntese de glicoproteínas. A síndrome CDG tipo 2E é caracterizada por dismorfismo, displasia esquelética, hipotonia, hepatoesplenomegalia, icterícia, insuficiência cardíaca, infecções recorrentes e epilepsia. Até o momento, foi descrito em dois bebês, ambos morreram nos primeiros três meses de vida. A síndrome é causada por uma mutação no gene que codifica COG-7 (cromossomo 16), uma subunidade do complexo oligomérico de Golgi | |||||||||||||||
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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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| Property / Canonical URI: https://id.who.int/icd/entity/808184224 / rank | |||||||||||||||
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CID11:ID_808184224 | |||||||||||||||
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dki-india-ID_808184224 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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16 August 2026
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| Property / Collection date: 16 August 2026 / rank | |||||||||||||||
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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.
| Language | Label | Description | Also known as |
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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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