MYH9-related disorder with sole presentation of end-stage kidney disease and long-term, recurrence-free living after living donor renal transplantation: a case report.

doi:10.1007/s13730-024-00892-0

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Article

MYH9-related disorder with sole presentation of end-stage kidney disease and long-term, recurrence-free living after living donor renal transplantation: a case report.

CEN case reports - 1 Feb 2025

Horibe Yuki, Yamanaka Kazuaki, Kaimori Junya, Miyata Yuji, Fukae Shota, Yoshida Takahiro, Nakagawa Masahiro, Ishihara Yasuki, Nagata Miho, Miyashita Yohei, Asano Yoshihiro, Kishikawa Hidefumi

Abstract excerpt

MYH9-related disorders are a group of autosomal dominant disorders caused by mutations in MYH9, and are characterized by thrombocytopenia, sensorineural hearing loss, cataracts, and renal failure. Here, we report a case of chronic renal failure due to MYH9-related disorder with renal symptoms in a patient who underwent living-donor renal transplantation. The patient was diagnosed with proteinuria during a health...

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Topics

Humans
Kidney Transplantation
Female
Kidney Failure, Chronic
Thrombocytopenia

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Living Donors

Adult

Hearing Loss, Sensorineural

Myosin Heavy Chains

Molecular Motor Proteins

Mutation

Glomerulosclerosis, Focal Segmental

Kidney

Source

Open in PubMed Open full text

Identifiers

PMID: 38831180
DOI: 10.1007/s13730-024-00892-0
PMCID: PMC11785911

Genes

MYH9

Provenance

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