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Article

Familial macro thrombocytopenia: role of genetics where morphology fails.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jul 2020

Chaudhary Himanshi, Jindal Ankur, Guleria Sandesh, Sharma Saniya, Sachdeva Man U S, Ahluwalia Jasmina

Abstract excerpt

: Myosin heavy chain 9 (MYH9)-related disorders are rare inherited platelet disorders that are accompanied by a wide variety of systemic abnormalities. The persistent thrombocytopenia is usually asymptomatic and these patients are often misdiagnosed and treated as immune thrombocytopenia. MYH9 gene has been studied in association with solid organ malignancies. We report a young girl with family history of...

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Identifiers

PMID: 32516168
DOI: 10.1097/MBC.0000000000000923

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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