What is included in the patient education about treatment of factor XIII (FXIII) deficiency?

Updated: Aug 01, 2019
  • Author: Robert A Schwartz, MD, MPH; Chief Editor: Perumal Thiagarajan, MD  more...
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Answer

Encourage patients to register with the local chapter of the National Hemophilia Foundation and to attend educational seminars. Provide one-on-one discussions of issues with patients and family members. Early and complete genetic testing can help families plan future pregnancies.

For patient education resources, see Bleeding Disorders.


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