Abstract
Afibrinogenemia is an extremely rare inherited bleeding disorder. Less than 100 such cases have been described from India. Beta-thalassemia carrier status (trait) is common in many Indian casts and religious groups; hence, a rare combination of these two conditions can be expected. Here, we report one such case treated solely using homeopathic medicine. The male patient was borne out of a nonconsanguineous marriage. He had delayed separation of the umbilical cord after 14 days and bleeding from the site. In addition, he had multiple bleeding episodes treated successfully by homeopathy since 11 months of age. His thalassemia trait needed no treatment. As fibrinogen concentrate is not easily available, this line of management could also be considered if the concentrate or safe cryoprecipitate is not immediately available.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.