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What is Congenital disorder of glycosylation type X -- Bombay blood group phenotype?

What is Congenital disorder of glycosylation type X -- Bombay blood group phenotype?

  • Congenital disorder of glycosylation type X -- Bombay blood group phenotype: A rare inherited disorder characterized by abnormal neutrophil functioning which reduces the body's immunity. The abnormal neutrophils are unable to be transported to sites of infection due to their inability to adhere to certain blood vessel components which would normally lead them to the infection site. Infections may be life-threatening as the body is unable to destroy bacteria effectively. Type 2 LAD is where neutrophils can't adhere to necessary blood vessel components due to the absence of proteins on the blood vessel walls needed to bind and guide the neutrophils to the infection site.

Congenital disorder of glycosylation type X -- Bombay blood group phenotype: Introduction

Types of Congenital disorder of glycosylation type X -- Bombay blood group phenotype:

Broader types of Congenital disorder of glycosylation type X -- Bombay blood group phenotype:

How serious is Congenital disorder of glycosylation type X -- Bombay blood group phenotype?

Complications of Congenital disorder of glycosylation type X -- Bombay blood group phenotype: see complications of Congenital disorder of glycosylation type X -- Bombay blood group phenotype

What causes Congenital disorder of glycosylation type X -- Bombay blood group phenotype?

Causes of Congenital disorder of glycosylation type X -- Bombay blood group phenotype: see causes of Congenital disorder of glycosylation type X -- Bombay blood group phenotype

What are the symptoms of Congenital disorder of glycosylation type X -- Bombay blood group phenotype?

Symptoms of Congenital disorder of glycosylation type X -- Bombay blood group phenotype: see symptoms of Congenital disorder of glycosylation type X -- Bombay blood group phenotype

Complications of Congenital disorder of glycosylation type X -- Bombay blood group phenotype: see complications of Congenital disorder of glycosylation type X -- Bombay blood group phenotype

Congenital disorder of glycosylation type X -- Bombay blood group phenotype: Testing

Diagnostic testing: see tests for Congenital disorder of glycosylation type X -- Bombay blood group phenotype.

Misdiagnosis: see misdiagnosis and Congenital disorder of glycosylation type X -- Bombay blood group phenotype.

How is it treated?

Doctors and Medical Specialists for Congenital disorder of glycosylation type X -- Bombay blood group phenotype: Medical Geneticist ; see also doctors and medical specialists for Congenital disorder of glycosylation type X -- Bombay blood group phenotype.
Treatments for Congenital disorder of glycosylation type X -- Bombay blood group phenotype: see treatments for Congenital disorder of glycosylation type X -- Bombay blood group phenotype

Name and Aliases of Congenital disorder of glycosylation type X -- Bombay blood group phenotype

Main name of condition: Congenital disorder of glycosylation type X -- Bombay blood group phenotype

Other names or spellings for Congenital disorder of glycosylation type X -- Bombay blood group phenotype:

CDG X [Bombay blood group phenotype], leukocyte adhesion deficiency, type 2

Congenital disorder of glycosylation type X -- Bombay blood group phenotype: Related Conditions

Research the causes of these diseases that are similar to, or related to, Congenital disorder of glycosylation type X -- Bombay blood group phenotype:

 

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