Congenital analbuminaemia (Q107767): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 14:48, 17 August 2026
Congenital analbuminaemia is characterised by the absence or dramatic reduction of circulating human serum albumin (HSA). Patients with congenital analbuminaemia present with only a few mild clinical signs and biochemical abnormalities including fatigue, low blood pressure, oedema, increased concentration of several plasma proteins and a prolonged albumin half-life.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1473391809 |
||
| English | Congenital analbuminaemia |
Congenital analbuminaemia is characterised by the absence or dramatic reduction of circulating human serum albumin (HSA). Patients with congenital analbuminaemia present with only a few mild clinical signs and biochemical abnormalities including fatigue, low blood pressure, oedema, increased concentration of several plasma proteins and a prolonged albumin half-life. |
Statements
CID11:ID_1473391809
0 references
dki-india-ID_1473391809
0 references
Concluído
0 references
