The surgical management of a patient with chronic renal failure and macrothrombocytopenia related to the MYH9 gene mutation: A case report-Reference-Cited by-同舟云学术

The surgical management of a patient with chronic renal failure and macrothrombocytopenia related to the MYH9 gene mutation: A case report

Published:2022-05-10 Issue:6 Volume:42 Page:651-656
ISSN:0275-1879
Container-title:Special Care in Dentistry
language:en
Short-container-title:Special Care in Dentistry

Author:

Costa Rafael Fiorese¹²,Bucharles Sérgio Gardano Elias²,Kagueiama Douglas Eiji²,Kus Cintia Pereira²,Andrade Ariane de Almeida²,Dirschnabel Acir José²,de Araujo Melissa Rodrigues¹,de Lima Antonio Adilson Soares¹

Affiliation:

1. Department of Stomatology, Universidade Federal do Paraná Curitiba PR Brazil

2. Fundação de Amparo a Pesquisa em Enfermidades Renais e Metabólicas Pró‐Renal Curitiba PR Brazil

Publisher

Wiley

Subject

General Dentistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/scd.12727

Reference26 articles.

1. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly

2. Epstein Syndrome

3. UntanuRV VajpayeeN.May Hegglin Anomaly. 2021 Jul 21. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan.

4. MYH9: Structure, functions and role of non-muscle myosin IIA in human disease

5. Renin-angiotensin system blockade is effective in reducing proteinuria of patients with progressive nephropathy caused by MYH9 mutations (Fechtner-Epstein syndrome)

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