A Fatal Neonatal Case of CHARGE Syndrome and Mini-Review of the Literature
Öz
Anahtar Kelimeler
Kaynakça
- 1. Issekutz KA, Graham Jr. JM, Prasad C, Smith IM, Blake KD. An epidemiological analysis of CHARGE syndrome: Preliminary results from a Canadian study. Am J Med Genet [Internet]. 2005;133A(3):309-17.
- 2. Janssen N, Bergman JEH, Swertz MA, Tranebjaerg L, Lodahl M, Schoots J, et al. Mutation Update on the CHD7 Gene Involved in CHARGE Syndrome. Human Mutation. 2012;33(8):1149-60.
- 3. Blake KD, Davenport SL, Hall BD, Hefner MA, Pagon RA, Williams MS, et al. CHARGE association: an update and review for the primary pediatrician. Clin Pediatr (Phila). 1998;37(3):159-73.
- 4. Verloes A. Updated diagnostic criteria for CHARGE syndrome: A proposal. Am J Med Genet. 2005;133A(3):306-8.
- 5. Hale CL, Niederriter AN, Green GE, Martin DM. Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria. Am J Med Genet A. 2016;170A(2):344-54.
- 6. Berube-Simard F-A, Pilon N. Molecular dissection of CHARGE syndrome highlights the vulnerability of neural crest cells to problems with alternative splicing and other transcription-related processes. Transcription. 2019;10(1):21-8.
- 7. Bajpai R, Chen DA, Rada-Iglesias A, Zhang J, Xiong Y, Helms J, et al. CHD7 cooperates with PBAF to control multipotent neural crest formation. Nature. 2010;463(7283):958-62.
- 8. Zentner GE, Layman WS, Martin DM, Scacheri PC. Molecular and phenotypic aspects of CHD7 mutation in CHARGE syndrome. Am J Med Genet Part A. 2010;152A:674–86.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Çocuk Sağlığı ve Hastalıkları
Bölüm
Olgu Sunumu
Yazarlar
Fatma Nur Sarı
0000-0003-4643-7622
Türkiye
Esra Sukran Cakar
0000-0001-5902-4582
Türkiye
Şehribanu Işık
0000-0003-2999-059X
Türkiye
Aybüke Yazıcı
0000-0001-9387-0029
Türkiye
Yayımlanma Tarihi
1 Ekim 2023
Gönderilme Tarihi
16 Aralık 2021
Kabul Tarihi
24 Nisan 2023
Yayımlandığı Sayı
Yıl 2023 Cilt: 20 Sayı: 3