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Behcet’s Syndrome

Behcet’s syndrome is a rare disease, which causes inflammation of blood vessels. Exact cause for the syndrome is not known. It is believed that an autoimmune disorder might be the cause for this...

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Crouzon syndrome

Crouzon syndrome is a genetic disorder. It is one of many birth defects that results in abnormal fusion between bones in the skull and face. Normally, as an infant’s brain grows, open sutures between...

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Edwards Syndrome

Edwards syndrome is a genetic disorder, in which a person has a third copy of material from chromosome 18, instead of the usual two copies. It is three times more common in girls than boys. The...

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Hemolytic uremic syndrome (HUS)

What is Hemolytic uremic syndrome ? Hemolytic uremic syndrome is a disorder that is caused due to anomalous and premature damage of red blood cells. The commencement of this process leads to the...

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Goldenhar Syndrome

What is Goldenhar Syndrome ? Goldenhar syndrome is a congenital condition that is characterized by abnormalities if the face, head and spine. Goldenhar syndrome is also referred to as...

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Fragile X Syndrome

What is Fragile X Syndrome ? It is one of the major types of inherited mental retardation. Fragile X Syndrome is caused due to mutation or alteration of a particular that is passed down in families....

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Morquio Syndrome

Morquio’s syndrome is a metabolic disorder that is inherited and wherein the body misses or lacks the essential ingredients that are necessary to break down elongated chains of sugar molecules known as...

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Chilblains – Pictures, Symptoms, Treatment, Causes

Chilblains, refers to a condition that is characterized by painful inflammation of the tiny blood vessels present in the skin. The disorder arises as a reaction of the skin to sudden warming after...

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Treacher Collins Syndrome

Treacher Collins syndrome is a rare genetic congenital condition that causes abnormal growth of facial tissues and bones. It tends to run in families and gets passed with an autosomal dominant...

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Turner Syndrome

Turner syndrome refers to a genetic disorder that is only found in girls. The most common features of people that suffer from the condition are shortness, nonfunctional ovaries, and certain physical...

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