Phosphomannoisomerase deficiency
Overview
Phosphomannose isomerase deficiency: Another name for Congenital disorder of glycosylation type 1B (or close medical condition association). Congenital disorder of glycosylation type 1B:
Symptoms
The list of signs and symptoms mentioned in various sources for Congenital disorder of glycosylation type 1B includes the 8 symptoms listed below: * Liver disease * Coagulopathy * Protein-losing enteropathy * Cyclic vomiting * Diarrhea * Hypoglycemia * Enlarged liver * Liver fibrosis Note that Congenital disorder of glycosylation type 1B symptoms usually refers to various symptoms known to a patient, but the phrase Congenital disorder of glycosylation type 1B signs may refer to those signs only noticable by a doctor.
Causes
Other Possible Causes of these Symptoms * Diarrhea * Enlarged liver * Hypoglycemia * Liver disease * Liver fibrosis
Diagnosis
These home medical tests may be relevant to Congenital disorder of glycosylation type 1B: * Child Behavior: Home Testing ADHD -- Home Testing, Concentration -- Home Testing * Cold & Flu: Home Testing: Home Fever Tests, Home Ear Infection Tests, Home Flu Tests