Congenital Platelet Disorder and Type I von Willebrand Disease Presenting as Prolonged Bleeding after Cleft Lip and Palate Repair

Author:

Pang John1,Zelken Jonathan1,Dorafshar Amir H.1,Strouse John J.1,Redett Richard1

Affiliation:

1. Plastic and Reconstructive Surgery, Johns Hopkins University School of Medicine.

Abstract

Cleft lip and palate can be associated with coagulopathy. Here, we report the first known case of congenital platelet disorder and von Willebrand disease presenting as prolonged bleeding after cleft lip and palate repair. After identifying the underlying pathology, platelet infusions and aminocaproic acid were given to decrease bleeding from a second surgical procedure. Whole exome sequencing identified a von Willebrand factor gene mutation, an adenine to guanine substitution at the c.475A location. A high index of suspicion should be had for coagulopathy in patients with syndromic cleft lip and palate.

Publisher

SAGE Publications

Subject

Otorhinolaryngology,Oral Surgery

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Komplikationen bei der Gaumenspalten-Chirurgie;Atlas der unerwünschten Ergebnisse in der Chirurgie von Lippen-Kiefer-Gaumenspalten;2023

2. Cleft Palate Surgery Complications;Atlas of Non-Desirable Outcomes in Cleft Lip and Palate Surgery;2022

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