Cholestasis - lymphoedema syndrome (Q64269): Difference between revisions
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Síndrome de colestase-linfedema é caracterizada por linfedema crônico grave e colestase neonatal grave que geralmente diminui durante a primeira infância e se torna episódica. Foi descrita em seis grandes famílias, principalmente da Noruega. A característica comum dessa condição autossômica recessiva é uma anomalia linfática generalizada. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1087517390 / rank | |||||||||||||||
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CID11:ID_1087517390 | |||||||||||||||
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dki-india-ID_1087517390 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 11:51, 14 August 2026
Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1087517390 |
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| English | Cholestasis - lymphoedema syndrome |
Cholestasis-lymphoedema syndrome is characterised by chronic severe lymphoedema and severe neonatal cholestasis that usually lessens during early childhood and becomes episodic. It has been described in six large families, mainly from Norway. The common feature of this autosomal recessive condition is a generalised lymphatic anomaly. |
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CID11:ID_1087517390
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dki-india-ID_1087517390
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Concluído
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13 August 2026
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