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Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding
Afibrinogenemia is an extremely rare bleeding disorder characterized by the absence or severe deficiency of fibrinogen, a major protein involved in the regulation of blood clotting. This disorder can have both hemorrhagic and/or thrombotic manifestations. We present the case of a female neonate who...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460120/ https://www.ncbi.nlm.nih.gov/pubmed/37637664 http://dx.doi.org/10.7759/cureus.42542 |
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author | Salah, Qais M AlRashayda, Rami R Heresh, Mohammad J Abulehya, Aya Salah Al-deen, Leena W |
author_facet | Salah, Qais M AlRashayda, Rami R Heresh, Mohammad J Abulehya, Aya Salah Al-deen, Leena W |
author_sort | Salah, Qais M |
collection | PubMed |
description | Afibrinogenemia is an extremely rare bleeding disorder characterized by the absence or severe deficiency of fibrinogen, a major protein involved in the regulation of blood clotting. This disorder can have both hemorrhagic and/or thrombotic manifestations. We present the case of a female neonate who was diagnosed with congenital afibrinogenemia within the first two weeks of life. The patient presented with persistent bleeding from the umbilical stump, prompting a thorough investigation and workup. Early diagnosis and management were essential to preventing life-threatening bleeding events. |
format | Online Article Text |
id | pubmed-10460120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
spelling | pubmed-104601202023-08-27 Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding Salah, Qais M AlRashayda, Rami R Heresh, Mohammad J Abulehya, Aya Salah Al-deen, Leena W Cureus Pediatrics Afibrinogenemia is an extremely rare bleeding disorder characterized by the absence or severe deficiency of fibrinogen, a major protein involved in the regulation of blood clotting. This disorder can have both hemorrhagic and/or thrombotic manifestations. We present the case of a female neonate who was diagnosed with congenital afibrinogenemia within the first two weeks of life. The patient presented with persistent bleeding from the umbilical stump, prompting a thorough investigation and workup. Early diagnosis and management were essential to preventing life-threatening bleeding events. Cureus 2023-07-27 /pmc/articles/PMC10460120/ /pubmed/37637664 http://dx.doi.org/10.7759/cureus.42542 Text en Copyright © 2023, Salah et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Pediatrics Salah, Qais M AlRashayda, Rami R Heresh, Mohammad J Abulehya, Aya Salah Al-deen, Leena W Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title | Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title_full | Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title_fullStr | Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title_full_unstemmed | Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title_short | Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding |
title_sort | early diagnosis and management of congenital afibrinogenemia: a case report of umbilical stump bleeding |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460120/ https://www.ncbi.nlm.nih.gov/pubmed/37637664 http://dx.doi.org/10.7759/cureus.42542 |
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