Congenital analbuminaemia (Q107767): Difference between revisions
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A analbuminemia congênita é caracterizada pela ausência ou redução drástica da albumina sérica humana circulante. Os pacientes com analbuminemia congênita apresentam apenas alguns sinais clínicos leves e anormalidades bioquímicas, incluindo fadiga, pressão arterial baixa, edema, concentração aumentada de várias proteínas plasmáticas e meia-vida prolongada da albumina. | |||
| description / en | description / en | ||
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. | |||
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 |
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| default for all languages | ID_1473391809 |
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| 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. |
