| Journal of Medical Cases, ISSN 1923-4155 print, 1923-4163 online, Open Access |
| Article copyright, the authors; Journal compilation copyright, J Med Cases and Elmer Press Inc |
| Journal website https://www.journalmc.org |
Case Report
Volume 11, Number 9, September 2020, pages 271-274
Congenital Factor VII Deficiency in Association With Bicuspid Aortic Valve and Multicystic Dysplastic Kidney Disease in a Child
Tables
| Test | Result | Reference |
|---|---|---|
| FEU: fibrinogen equivalent units. | ||
| Hemoglobin (Hb) | 15.8 g/dL | 12.5 - 20.5 |
| Prothrombin time (PT) | 37.5 s | 10.3 - 14 |
| Activated prothrombin time (aPTT) | 35.1 s | 29 - 40 |
| International normalized ratio (INR) | 3.9 | 0.9 - 1.15 |
| Factor VII level | 0.07 | 0.7 - 1.2 |
| D-dimer | 0.4 mg/L FEU | 0.17 - 0.64 |
| Fibrinogen | 413.9 mg/dL | 160 - 350 |
| Age/study | Gender | Association |
|---|---|---|
| Two years [9] | Female | Hirschsprung disease |
| Seven years [13] | Male | Factor X deficiency |
| Twenty-one years [15] | Female | Protein C deficiency and pulmonary artery stenosis |
| Infant [16] | Male | Pulmonary atresia and hypoplastic right ventricle |
| Five weeks [17] | Unknown | Langdon down syndrome, complete endocardial cushion defect, and tetralogy of Fallot |
| Seventy-eight years [18] | Female | Severe aortic stenosis |
| Three years [19] | Unknown | Cleft palate |
| Thirty-two years [20] | Female | Autoimmune hepatitis type II and Grave’s disease |
| Twenty days [21] | Male | Chairi malformation |
| Seven and twelve years (siblings) [22] | Unknown | Hereditary spastic paraplegia |
| Twenty-five years [23] | Female | Jaw deformity |
| Forty-eight years [24] | Female | Neuroendocrine ampullary tumor |
| Unknown [25] | Unknown | Kidney stone |
| Two months [26] | Female | Anterior segment dysgenesis |
| Forty-one years [27] | Female | Multiple cerebral aneurysms |
| Two months [28] | Male | Inguinal hernia |
| Nine years [29] | Male | Partial monosomy of 13q and trisomy of 16p |