Genotype-phenotype correlation in MYH9-related thrombocytopenia

Fan Dong, Sufeng Li, Núria Pujol-Moix, Naomi L C Luban, Sang Won Shin, Jae Hong Seo, Arlette Ruiz-Saez, J. Demeter, Scott Langdon, Michael J. Kelley

Research output: Article

70 Citations (Scopus)

Abstract

Mutation of the non-muscle myosin heavy chain type II-A results in MYH9-related hereditary macrothrombocytopenia (HMTC), including four autosomal dominant platelet disorders: May-Hegglin anomaly (MHA), Sebastian (SBS), Fechtner (FS) and Epstein (EPS) syndrome. Denaturing high-performance liquid chromatography (DHPLC) was optimised for rapid screening of the seven exons harbouring all but one of the previously reported mutations of MYH9. Individuals from 13 families with phenotypes suggestive of MYH9-related HMTC were screened for mutations by DHPLC followed by direct sequencing of samples with aberrant column retention time. Mutations were identified in all 13 families. Six distinct missense heterozygous mutations were found in 10 families, including six families with MHA or SBS (E1841K, D1424N), three families with FS (R702H, R1165C, and D1424Y), and one family with EPS (S96L). A truncating mutation (R1933X) was found in three MHA families. A review of all published mutations suggests that mutation in the C-terminal coiled coil region or truncation of the tailpiece is associated with haematological-only phenotype, while mutation of the head ATPase domain frequently is associated with nephropathy and/or hearing loss. Mutations of other regions have intermediate expression of non-haematological characteristics. Further study is required to confirm these associations and understand the molecular basis for this genotype-phenotype relationship.

Original languageEnglish
Pages (from-to)620-627
Number of pages8
JournalBritish Journal of Haematology
Volume130
Issue number4
DOIs
Publication statusPublished - aug. 2005

Fingerprint

Genetic Association Studies
Thrombocytopenia
Mutation
Phenotype
High Pressure Liquid Chromatography
Myosin Heavy Chains
Missense Mutation
Hearing Loss
Adenosine Triphosphatases
Exons
Blood Platelets
Head
Genotype
MYH9-Related Disorders

ASJC Scopus subject areas

  • Hematology

Cite this

Dong, F., Li, S., Pujol-Moix, N., Luban, N. L. C., Shin, S. W., Seo, J. H., ... Kelley, M. J. (2005). Genotype-phenotype correlation in MYH9-related thrombocytopenia. British Journal of Haematology, 130(4), 620-627. https://doi.org/10.1111/j.1365-2141.2005.05658.x

Genotype-phenotype correlation in MYH9-related thrombocytopenia. / Dong, Fan; Li, Sufeng; Pujol-Moix, Núria; Luban, Naomi L C; Shin, Sang Won; Seo, Jae Hong; Ruiz-Saez, Arlette; Demeter, J.; Langdon, Scott; Kelley, Michael J.

In: British Journal of Haematology, Vol. 130, No. 4, 08.2005, p. 620-627.

Research output: Article

Dong, F, Li, S, Pujol-Moix, N, Luban, NLC, Shin, SW, Seo, JH, Ruiz-Saez, A, Demeter, J, Langdon, S & Kelley, MJ 2005, 'Genotype-phenotype correlation in MYH9-related thrombocytopenia', British Journal of Haematology, vol. 130, no. 4, pp. 620-627. https://doi.org/10.1111/j.1365-2141.2005.05658.x
Dong, Fan ; Li, Sufeng ; Pujol-Moix, Núria ; Luban, Naomi L C ; Shin, Sang Won ; Seo, Jae Hong ; Ruiz-Saez, Arlette ; Demeter, J. ; Langdon, Scott ; Kelley, Michael J. / Genotype-phenotype correlation in MYH9-related thrombocytopenia. In: British Journal of Haematology. 2005 ; Vol. 130, No. 4. pp. 620-627.
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AU - Seo, Jae Hong

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