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Case 4: Hydrocephalus, Macrothrombocytopenia, Inclusion Bodies, and Nephropathy in a 9-year-old Boy.

Belal TA, Al Menabawy NM. Belal TA, et al. Pediatr Rev. 2017 Jul;38(7):335-336. doi: 10.1542/pir.2016-0235. Pediatr Rev. 2017. PMID: 28667238 No abstract available.

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Epstein syndrome with rapid progression to end stage renal disease.

Alhindawi E, Al-Jbour S. Alhindawi E, et al. Saudi J Kidney Dis Transpl. 2009 Nov;20(6):1076-8. Saudi J Kidney Dis Transpl. 2009. PMID: 19861875 Free article.

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MYH9 Disorders (May-Hegglin Anomaly) the Role of the Blood Smear.

Barros Pinto MP, Marques G. Barros Pinto MP, et al. J Pediatr Hematol Oncol. 2019 Apr;41(3):228. doi: 10.1097/MPH.0000000000001441. J Pediatr Hematol Oncol. 2019. PMID: 30807393

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Sporadic Epstein syndrome with macrothrombocytopenia, sensorineural hearing loss and renal failure.

Makino S, Kunishima S, Ikumi A, Awaguni H, Shinozuka J, Tanaka S, Maruyama R, Imashuku S. Makino S, et al. Pediatr Int. 2015 Oct;57(5):977-81. doi: 10.1111/ped.12736. Epub 2015 Sep 21. Pediatr Int. 2015. PMID: 26387855

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Nephroquiz 10: A 16-Year-Old Patient With Thrombocytopenia and Kidney Failure.

Ghazizadeh M, Ghazizadeh M, Nafar M. Ghazizadeh M, et al. Iran J Kidney Dis. 2017 Nov;11(6):469-471. Iran J Kidney Dis. 2017. PMID: 29190609 Free article. No abstract available.

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Familial macro thrombocytopenia: role of genetics where morphology fails.

Chaudhary H, Jindal A, Guleria S, Sharma S, Sachdeva MUS, Ahluwalia J. Chaudhary H, et al. Blood Coagul Fibrinolysis. 2020 Jul;31(5):333-334. doi: 10.1097/MBC.0000000000000923. Blood Coagul Fibrinolysis. 2020. PMID: 32516168

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[Renal diseases related to MYH9 disorders].

Galeano D, Zanoli L, L'Imperio V, Fatuzzo P, Granata A. Galeano D, et al. G Ital Nefrol. 2017 Apr;34(2):40-57. G Ital Nefrol. 2017. PMID: 28682562 Review. Italian.

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MYH9-Related Thrombocytopenia.

Ban BH, Shah V. Ban BH, et al. Mayo Clin Proc. 2017 Jul;92(7):1169-1170. doi: 10.1016/j.mayocp.2017.05.003. Mayo Clin Proc. 2017. PMID: 28688473 No abstract available.

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Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.

Suzuki N, Kunishima S, Ikejiri M, Maruyama S, Sone M, Takagi A, Ikawa M, Okabe M, Kojima T, Saito H, Naoe T, Matsushita T. Suzuki N, et al. PLoS One. 2013 Aug 20;8(8):e71187. doi: 10.1371/journal.pone.0071187. eCollection 2013. PLoS One. 2013. PMID: 23976996 Free PMC article.

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An interesting case of thrombocytopenia in pregnancy.

Garcia-Horton A, Chin-Yee I, Lam S. Garcia-Horton A, et al. Int J Hematol. 2020 Aug;112(2):139-140. doi: 10.1007/s12185-020-02922-w. Epub 2020 Jun 19. Int J Hematol. 2020. PMID: 32557127 No abstract available.

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