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Gastroschisis- Overview, Diagnosis and Treatment

Definition Gastroschisis is a relatively uncommon condition that occurs in approximately 1 in 5,000 live births. It is one of a group of birth defects known as abdominal wall defects, which occur very early in gestation and are characterized by an opening in the abdominal wall of the fetus. Most …

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Gastroparesis- Definition, Causes, and Treatment

Definition Gastroparesis means partial paralysis of the stomach. The word ‘gastro’ refers to the stomach, and the word ‘paresis’ means partial paralysis. To understand what goes wrong in gastroparesis, it is important to know how a healthy digestive tract functions. When we eat, we start by chewing and swallowing (ingesting), …

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Gricelli Syndrome – Causes, Diagnosis, and Treatment.

Gricelli Syndrome – Overview Gricelli syndrome is an inherited condition characterized by unusually light (hypopigmented) skin and light silvery-gray hair starting in infancy. Researchers have identified three types of this disorder, which are distinguished by their genetic cause and pattern of signs and symptoms. Griscelli syndrome type 1 involves severe …

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Gigantism – Definition, Causes, and Treatment.

Definition of Gigantism Gigantism is a rare condition that causes abnormal growth in children. This change is most notable in terms of height, but girth is affected as well. It occurs when your child’s pituitary gland makes too much growth hormone, which is also known as somatotropin. Early diagnosis is …

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Gangrene – Causes, Symptoms, and Treatment

What is gangrene?   Gangrene, which refers to tissue death caused by a severe shortage of blood supply or serious bacterial infection, occurs in lower extremities. It is more common in the toes than other parts of the body. Gangrene tends to happen more often among people with peripheral artery …

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Galactosemia – Definition, Causes, and Prevention.

Definition Galactosemia is a rare, hereditary disorder of carbohydrate metabolism that affects the body’s ability to convert galactose (a sugar contained in milk, including human mother’s milk) to glucose (a different type of sugar). The disorder is caused by a deficiency of an enzyme galactose-1-phosphate uridyl transferase (GALT) which is …

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