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SEQUENCING: Congenital Neutropenia Sample shipping address:Sample dropoff locations:Washington University Department of Pathology & Immunology Clinical Support Office 425 S. Euclid Ave. | MSC 8024144711
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Individuals who have been diagnosed with congenital neutropenia, a rare genetic disorder characterized by a low level of white blood cells called neutrophils, may require specialized care from healthcare professionals.
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Congenital neutropenia is a rare genetic disorder characterized by a significantly reduced number of neutrophils, a type of white blood cell essential for fighting off infections.
Individuals diagnosed with congenital neutropenia may be required to file for specific medical treatments or health documentation, often involving healthcare providers or medical institutions responsible for their care.
Filling out information related to congenital neutropenia generally involves providing personal health details, treatment history, and any relevant genetic information on medical forms that are specified by healthcare providers.
The purpose of recognizing congenital neutropenia is to identify and manage the patient's risk of infections, understand the genetic basis of the disorder, and provide appropriate medical care.
Reports on congenital neutropenia should include patient demographics, medical history, genetic testing results, neutrophil counts, and any treatment plans.
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