The following Conditions are related to Stomach pain
Select a specific condition below to view its details.
- Fabry disease
A parent can pass on the faulty gene that causes Fabry disease to a child.Fabry Disease, Anderson-Fabry disease or lysosomal storage disease is an inherited disorder.Children inherit a mutated galactosidase alpha -GLA gene on the X chromosome from a parent.The GLA gene produces an alpha-GAL enzyme that helps break down fatty substances -sphingolipids.People who inherit a defective GLA Read More
- Glycolipid lipidosis
Glycolipid lipidosis is known as Fabry disease. It is caused by mutation or deficiency in galaactosidase-GLA located in X- Chromosomes and by abnormal accumulations of neutral glycolipids in blood vessel cells.This is a generic disorder that passes through gene mutation from parents, males with X-chromosomes linked by Fabry disease that passes GLA gene to all their Daughters but never to sons.But Females h Read More
- Hereditary spherocytosis (hs)
HS is divided into mild, moderate, and severe forms of the disease. Classification is based on the amounts of hemoglobin, reticulocytes, and bilirubin and the amount of spectrin in red blood cells. Hemoglobin transports oxygen in the blood. Reticulocytes are immature red blood cells. Bilirubin is formed in the liver when hemoglobin is broken down. Spectrin is a protein that helps keep the shape of a cell. Decreased hemoglobin and spectrin and Read More