Difference between revisions of "DICER1 syndrome"

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*[[Cystic nephroma, pediatric type]].<ref name=pmid26772403>{{cite journal |authors=Cajaiba MM, Khanna G, Smith EA, Gellert L, Chi YY, Mullen EA, Hill DA, Geller JI, Dome JS, Perlman EJ |title=Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations |journal=Hum Pathol |volume=48 |issue= |pages=81–7 |date=February 2016 |pmid=26772403 |pmc=4979561 |doi=10.1016/j.humpath.2015.08.022 |url=}}</ref><ref name=pmid28222777>{{cite journal |authors=Fernández-Martínez L, Villegas JA, Santamaría Í, Pitiot AS, Alvarado MG, Fernández S, Torres H, Paredes Á, Blay P, Balbín M |title=Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree |journal=BMC Cancer |volume=17 |issue=1 |pages=146 |date=February 2017 |pmid=28222777 |pmc=5320664 |doi=10.1186/s12885-017-3136-5 |url=}}</ref>
*[[Cystic nephroma, pediatric type]].<ref name=pmid26772403>{{cite journal |authors=Cajaiba MM, Khanna G, Smith EA, Gellert L, Chi YY, Mullen EA, Hill DA, Geller JI, Dome JS, Perlman EJ |title=Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations |journal=Hum Pathol |volume=48 |issue= |pages=81–7 |date=February 2016 |pmid=26772403 |pmc=4979561 |doi=10.1016/j.humpath.2015.08.022 |url=}}</ref><ref name=pmid28222777>{{cite journal |authors=Fernández-Martínez L, Villegas JA, Santamaría Í, Pitiot AS, Alvarado MG, Fernández S, Torres H, Paredes Á, Blay P, Balbín M |title=Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree |journal=BMC Cancer |volume=17 |issue=1 |pages=146 |date=February 2017 |pmid=28222777 |pmc=5320664 |doi=10.1186/s12885-017-3136-5 |url=}}</ref>


Others:
*[[Embryonal rhabdomyosarcoma]].<ref>{{cite journal |authors=Apellaniz-Ruiz M, McCluggage WG, Foulkes WD |title=DICER1-associated embryonal rhabdomyosarcoma and adenosarcoma of the gynecologic tract: Pathology, molecular genetics, and indications for molecular testing |journal=Genes Chromosomes Cancer |volume=60 |issue=3 |pages=217–233 |date=March 2021 |pmid=33135284 |doi=10.1002/gcc.22913 |url=}}</ref>
==References==
==References==
{{Reflist|1}}
{{Reflist|1}}


[[Category:Syndromes]]
[[Category:Syndromes]]

Revision as of 12:33, 24 March 2024

DICER1 syndrome is characterized by mutations in the DICER1 gene.

Conditions associated with the syndrome include:

Others:

References

  1. ↑ 1.0 1.1 van Engelen, K.; Villani, A.; Wasserman, JD.; Aronoff, L.; Greer, MC.; Tijerin Bueno, M.; Gallinger, B.; Kim, RH. et al. (Jan 2018). "DICER1 syndrome: Approach to testing and management at a large pediatric tertiary care center.". Pediatr Blood Cancer 65 (1). doi:10.1002/pbc.26720. PMID 28960912.
  2. ↑ Bueno, MT.; Martínez-Ríos, C.; la Puente Gregorio, A.; Ahyad, RA.; Villani, A.; Druker, H.; van Engelen, K.; Gallinger, B. et al. (Sep 2017). "Pediatric imaging in DICER1 syndrome.". Pediatr Radiol 47 (10): 1292-1301. doi:10.1007/s00247-017-3875-0. PMID 28474256.
  3. ↑ de Kock, L.; Terzic, T.; McCluggage, WG.; Stewart, CJR.; Shaw, P.; Foulkes, WD.; Clarke, BA. (Sep 2017). "DICER1 Mutations Are Consistently Present in Moderately and Poorly Differentiated Sertoli-Leydig Cell Tumors.". Am J Surg Pathol 41 (9): 1178-1187. doi:10.1097/PAS.0000000000000895. PMID 28654427.
  4. ↑ Cajaiba MM, Khanna G, Smith EA, Gellert L, Chi YY, Mullen EA, Hill DA, Geller JI, Dome JS, Perlman EJ (February 2016). "Pediatric cystic nephromas: distinctive features and frequent DICER1 mutations". Hum Pathol 48: 81–7. doi:10.1016/j.humpath.2015.08.022. PMC 4979561. PMID 26772403. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4979561/.
  5. ↑ Fernández-Martínez L, Villegas JA, Santamaría Í, Pitiot AS, Alvarado MG, Fernández S, Torres H, Paredes Á, Blay P, Balbín M (February 2017). "Identification of somatic and germ-line DICER1 mutations in pleuropulmonary blastoma, cystic nephroma and rhabdomyosarcoma tumors within a DICER1 syndrome pedigree". BMC Cancer 17 (1): 146. doi:10.1186/s12885-017-3136-5. PMC 5320664. PMID 28222777. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320664/.
  6. ↑ Apellaniz-Ruiz M, McCluggage WG, Foulkes WD (March 2021). "DICER1-associated embryonal rhabdomyosarcoma and adenosarcoma of the gynecologic tract: Pathology, molecular genetics, and indications for molecular testing". Genes Chromosomes Cancer 60 (3): 217–233. doi:10.1002/gcc.22913. PMID 33135284.
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