Congenital analbuminaemia (Q107767)
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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
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