1. A case of inherited type 1 and type 2A von Willebrand disease confirmed by diagnostic exome sequencing
- Author
-
Jung-Sook Ha, Ja-Hyun Jang, Heung Sik Kim, Ye Jee Shim, So Yun Park, and Nani Jung
- Subjects
Male ,0301 basic medicine ,Heterozygote ,congenital, hereditary, and neonatal diseases and abnormalities ,medicine.medical_specialty ,medicine.medical_treatment ,von Willebrand Disease, Type 2 ,030204 cardiovascular system & hematology ,Compound heterozygosity ,von Willebrand Disease, Type 1 ,Gastroenterology ,03 medical and health sciences ,Exon ,0302 clinical medicine ,Desmopressin Injection ,Von Willebrand factor ,hemic and lymphatic diseases ,Internal medicine ,Exome Sequencing ,medicine ,Von Willebrand disease ,Coagulopathy ,Humans ,Child ,Exome sequencing ,biology ,business.industry ,Hematology ,medicine.disease ,Pedigree ,030104 developmental biology ,Palatoplasty ,Oncology ,Pediatrics, Perinatology and Child Health ,biology.protein ,business - Abstract
A 10-year-old male and his family members visited a pediatric hematology clinic due to coagulopathy. Laboratory tests indicated von Willebrand disease (vWD) in all the family members. We conducted diagnostic exome sequencing for confirmation. The patient was confirmed to be a compound heterozygote for vWD: c.2574C > G (p.Cys858Trp) from his father (known variant of vWD type 1) and c.3390C > T (p.Pro1127_Gly1180delinsArg) from his mother (variant known to result in exon 26 skipping in vWD type 2A). He was managed with factor VIII and von Willebrand factor complex concentrate during palatoplasty due to bleeding despite pre-operative desmopressin injection. The operation was completed successfully.
- Published
- 2018
- Full Text
- View/download PDF