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The case of Waardenburg syndrome type II caused of nonsense-variant of the MITF gene in the context of the epigenetic mosaicism hypothesis

https://doi.org/10.25789/YMJ.2021.76.28

About the Authors

F. M. Teryutin
FSBSI YSC CMP
Russian Federation

Teryutin Fedor Mikhailovich – MD, senior researche



N. A. Barashkov
FSBSI YSC CMP
Russian Federation

Barashkov Nikolay Alekseevich – PhD, head of laboratory



N. A. Lebedeva
Medical Institute FSASI NEFU named after M.K. Ammosov
Russian Federation

Lebedeva Natalia Afanasyevna – MD



References

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3. Happle R. Can Waardenburg syndrome type 2 be explained by epigenetic mosaicism? / R. Happle // Am J Med Genet. 2021; 185A:1304–1306. DOI: 10.1002/ajmg.a.62075

4. Hearing loss in Waardenburg syndrome: a systematic review / J. Song, Y. Feng, F.R. Acke [et al.] // Clin. Genet. 2016; V. 89. Issue 4. P.416-425. DOI: 10.1111/cge.12631

5. Mutation at the an ophthalmic white locus in Syrian hamsters: haploinsuficiency in the Mitf gene mimics human Waardenburg syndrome type 2 / Hodgkinson C.A., Nakayama A., Li H. [et al.] // Hum. Mol. Genet. 1998; V.7. Issue 4. P.703–708.

6. Nayak C.S., Isaacson G. Worldwide distribution of Waardenburg syndrome / Nayak C.S., Isaacson G. // Ann. Otol. Rhinol. Laryngol. 2003; V.112. P.817–820. DOI: 10.1177/000348940311200913

7. Pigmentary disorders in association with congenital deafness / W.B. Reed, V.M. Stone, E. Boder, L. Ziprkowski // Arch. Dermatol. 1967; V.95. Issue 2. P.176–186. DOI:10.1001/archderm.1967.01600320032005

8. Read A.P. Waardenburg syndrome / A.P. Read, V.E. Newton // J. Med. Genet. 1997; V.34. Issue 8. P.656–665. DOI: 10.1136/jmg.34.8.656

9. The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndroms / I.Y. Iourov, S.G. Vorsanova, O.S. Kurinnaya [et al.] // Journal of neurology and psychiatry. 2014; 114(1). 49-53.

10. The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families / Q. Liu, J. Cheng, Y. Lu [et al.] // Int. j. Pediatr. Otorinolaryngol. 2020; Mar; 130:109806. DOI: 10.1016/j.ijporl.2019.109806.

11. Waardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium / L.A. Farrer, K.M. Grundfast, J. Amos [et al.] //Am. J. Hum. Genet. 1992; V.50. Issue 5. P.902–913.

12. Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations / X.-P. Wang, Y.-L. Liu, L.-Y. Mei [et al.] // Journal of Human Genetics. 2018; March. 63:639–646. DOI:10.1038/s10038-018-0425-z


Review

For citations:


Teryutin F.M., Barashkov N.A., Lebedeva N.A. The case of Waardenburg syndrome type II caused of nonsense-variant of the MITF gene in the context of the epigenetic mosaicism hypothesis. Yakut Medical Journal. 2021;(4):118-119. https://doi.org/10.25789/YMJ.2021.76.28

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ISSN 1813-1905 (Print)
ISSN 2312-1017 (Online)