Hennekam lymphangiectasia-lymphoedema syndrome (Q99531): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| (One intermediate revision by the same user not shown) | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 16:12, 16 August 2026
Hennekam lymphangiectasia-lymphoedema syndrome (Hennekam syndrome) is characterised by the association of lymphoedema, intestinal lymphangiectasia, intellectual deficit and facial dysmorphism. Lymphoedema affects the face, lower limbs and genitalia; if not present at birth, it tends to appear by early infancy. Intestinal lymphangiectasia may result in protein-losing enteropathy, growth retardation, peripheral oedema and ascites. Facial signs include a flat face, a broad and depressed nasal bridge, hypertelorism, epicanthal folds, a small mouth, and low-set ears.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_162216708 |
||
| English | Hennekam lymphangiectasia-lymphoedema syndrome |
Hennekam lymphangiectasia-lymphoedema syndrome (Hennekam syndrome) is characterised by the association of lymphoedema, intestinal lymphangiectasia, intellectual deficit and facial dysmorphism. Lymphoedema affects the face, lower limbs and genitalia; if not present at birth, it tends to appear by early infancy. Intestinal lymphangiectasia may result in protein-losing enteropathy, growth retardation, peripheral oedema and ascites. Facial signs include a flat face, a broad and depressed nasal bridge, hypertelorism, epicanthal folds, a small mouth, and low-set ears. |
Statements
CID11:ID_162216708
0 references
dki-india-ID_162216708
0 references
Concluído
0 references
15 August 2026
0 references
