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Article

Renal manifestations of patients with MYH9-related disorders.

Pediatric nephrology (Berlin, Germany) - 1 Apr 2011

Han Kyoung Hee, Lee HyunKyung, Kang Hee Gyung, Moon Kyung Chul, Lee Joo Hoon, Park Young Seo, Ha Il Soo, Ahn Hyo Seop, Choi Yong, Cheong Hae Il

Abstract excerpt

MYH9-related disorders are a group of autosomal, dominantly inherited disorders caused by mutations of the MYH9 gene, which encodes the non-muscle myosin heavy chain IIA (NMMHC-IIA). May-Hegglin anomaly and Sebastian, Fechtner, and Epstein syndromes belong to this group. Macrothrombocytopenia is a common characteristic associated with MYH9-related disorders, and basophilic cytoplasmic inclusion bodies in...

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Source

Identifiers

PMID: 21210153
DOI: 10.1007/s00467-010-1735-3

Genes

MYH9

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

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Renal manifestations of patients with MYH9-related disorders.PMID 21210153Read ↗

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A notable case report of May-Hegglin anomaly with immune complex-related nephropathy: a genetic and histological analysis.Semantic proximity Read ↗

Management of patients with severe Epstein syndrome: Review of four patients who received living-donor renal transplantation.Semantic proximity Read ↗

Successful living-related kidney transplantation in MYH9-related disorder with macrothrombocytopenia: lessons for the clinical nephrologist.Semantic proximity Read ↗

MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.Semantic proximity Read ↗

Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure: case report and review of the literature.Semantic proximity Read ↗

Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome).Semantic proximity Read ↗

Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease.Semantic proximity Read ↗

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