HomeGenetic Disorders Information Center: List of Different types of Genetic Disorders

Genetic Disorders Information Center: List of Different types of Genetic Disorders

What Are The Complications Of Lynch Syndrome?

What Are The Complications Of Lynch Syndrome? The complications that can occur with lynch syndrome (LS) are the increase risk of getting the following cancers....

What Are The First Symptoms Of Lynch Syndrome?

What Are The First Symptoms Of Lynch Syndrome? There are no first symptoms for Lynch syndrome. Lynch syndrome (LS) or Hereditary Non-polyposis Colorectal Cancer (HNPCC)...

What Is The Prognosis For Lynch Syndrome?

What Is The Prognosis For Lynch Syndrome? Lynch syndrome or hereditary non polyposis colorectal cancers (HNPCC) prognosis depends on whether the patient will get a...

Who Is At Risk Of Lynch Syndrome?

Lynch syndrome is a genetic condition, it’s an autosomal dominant condition which occur due to mutations in certain genes. Therefore, there are no specific...

How Is MCAD Deficiency Diagnosed?

MCAD deficiency is a genetically inherited disorder. MCAD stands for medium-chain acyl-CoA dehydrogenase. It is an autosomal recessive disorder. It is a disorder related...

What Are The Symptoms Of MCAD Deficiency?

MCAD deficiency is a condition in which the body is unable to break down some of the fatty acids, especially medium chain fatty acids,...

Why Does MCAD Deficiency Cause Hypoglycemia?

MCAD is a genetically inherited disorder. It is an autosomal recessive disorder that is transferred to a child only if both parents contribute one...

How To Prevent MCAD Deficiency?

MCAD deficiency, also known as medium chain acyl CoA dehydrogenase deficiency, is a genetically inherited disorder. It is an autosomal recessive disorder. The characteristic...

Life Expectancy For MCAD Deficiency

MCAD deficiency (MCADD), also known as medium chain acyl CoA dehydrogenase, is an inherited disorder. It is a genetically autosomal recessive disorder, that is...

Natural Remedies For MCAD Deficiency

MCAD deficiency (MCADD) or medium chain acyl CoA dehydrogenase deficiency is a genetically inherited autosomal recessive disorder and is caused due to mutations in...
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