Periodontal Disease in Two Siblings with VPS45-associated Severe Congenital Neutropenia Type V: A Case Report
- PMID: 33623350
- PMCID: PMC7887162
- DOI: 10.5005/jp-journals-10005-1841
Periodontal Disease in Two Siblings with VPS45-associated Severe Congenital Neutropenia Type V: A Case Report
Abstract
VPS45-associated severe congenital neutropenia type V (VPS45-associated SCN5) is an autosomal recessive disorder caused by defective endosomal intracellular protein trafficking due to mutations in VPS45 underlies a reduced absolute neutrophil count >500 cells/mm3 and impaired neutrophil function. VPS45-associated SCN5 is a very rare condition with only 19 patients previously reported in the literature. Patients suffering from this disorder having profound neutropenia in the first months of life, fever, pneumonitis, skin infections, oral ulcerations, and gingivitis. This paper reports the first two cases of VPS45-associated SCN5 in Saudi Arabia and describes the treatment approaches for periodontal disease as a manifestation of that disorder since the existing dental literature is lacking sufficient information on the management of those kinds of patients. The present two cases reflect the importance of early diagnosis of periodontal disease as a possible indicator of underlying systemic disease.
How to cite this article: Alotaibi FA, Albarkheel AI. Periodontal Disease in Two Siblings with VPS45-associated Severe Congenital Neutropenia Type V: A Case Report. Int J Clin Pediatr Dent 2020;13(5):572-575.
Keywords: Periodontal disease; Severe congenital neutropenia; VPS45.
Copyright © 2020; Jaypee Brothers Medical Publishers (P) Ltd.
Conflict of interest statement
Source of support: Nil Conflict of interest: None
Figures




Similar articles
-
A humanized Caenorhabditis elegans model for studying pathogenic mutations in VPS45, a protein essential for membrane trafficking, associated with severe congenital neutropenia.MicroPubl Biol. 2023 Nov 27;2023:10.17912/micropub.biology.001052. doi: 10.17912/micropub.biology.001052. eCollection 2023. MicroPubl Biol. 2023. PMID: 38089934 Free PMC article.
-
A congenital neutrophil defect syndrome associated with mutations in VPS45.N Engl J Med. 2013 Jul 4;369(1):54-65. doi: 10.1056/NEJMoa1301296. Epub 2013 Jun 5. N Engl J Med. 2013. PMID: 23738510 Free PMC article.
-
A novel homozygous VPS45 p.P468L mutation leading to severe congenital neutropenia with myelofibrosis.Pediatr Blood Cancer. 2017 Sep;64(9). doi: 10.1002/pbc.26571. Epub 2017 Apr 28. Pediatr Blood Cancer. 2017. PMID: 28453180
-
How we approach: Severe congenital neutropenia and myelofibrosis due to mutations in VPS45.Pediatr Blood Cancer. 2019 Jan;66(1):e27473. doi: 10.1002/pbc.27473. Epub 2018 Oct 7. Pediatr Blood Cancer. 2019. PMID: 30294941 Free PMC article. Review.
-
Oral findings and clinical implications of patients with congenital neutropenia: a literature review.Turk J Pediatr. 2013 May-Jun;55(3):241-5. Turk J Pediatr. 2013. PMID: 24217068 Review.
References
Publication types
LinkOut - more resources
Full Text Sources