Congenital Analbuminemia
Table of contents:
Description
Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).
Clinical Features
Top most frequent phenotypes and symptoms related to Congenital Analbuminemia
- Neoplasm
- Fatigue
- Edema
- Osteoporosis
- Carcinoma
- Small for gestational age
- Hypotension
- Hyperlipidemia
- Atherosclerosis
- Hypercholesterolemia
And another 4 symptoms. If you need more information about this disease we can help you.
Click here to know more about Mendelian.
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Congenital Analbuminemia Recommended genes panels
| Panel Name, Specifity and genes Tested/covered |
|---|
 Analbuminemia (sequence analysis of ALB gene).
By CGC Genetics (Portugal).
ALB
Specificity
100 %
Genes
100 % |
|
Analbuminemia (sequence analysis of ALB gene).
By CGC Genetics (Portugal).
ALB
Specificity
100 %
Genes
100 % |
 ALB.
By Fulgent Genetics Fulgent Genetics (United States).
ALB
Specificity
100 %
Genes
100 % |
You can get up to -5 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
OMIM ORPHANET Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TREHALASE DEFICIENCY CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A; CMT2A2A CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, MYOPATHIC, STRESS-INDUCED