MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura.

Yilmaz Keskin, Ebru; Yüceer, Ramazan O; Baspinar, Sirin; Okur, Erdogan; Berdeli, Afig

Yilmaz Keskin, Ebru; Yüceer, Ramazan O; Baspinar, Sirin; Okur, Erdogan; Berdeli, Afig.

Affiliation

Yilmaz Keskin E; Departments of Pediatric Hematology and Oncology.
Yüceer RO; Pathology.
Baspinar S; Pathology.
Okur E; Otorhinolaryngology-Head and Neck Surgery, Süleyman Demirel University Medical Faculty, Isparta.
Berdeli A; Molecular Medicine Laboratory, Department of Pediatrics, Ege University Medical Faculty, Izmir, Turkey.

J Pediatr Hematol Oncol ; 43(8): e1265-e1266, 2021 Nov 01.

Article in En | MEDLINE | ID: mdl-34310475

Subject(s)

Hearing Loss, Sensorineural/pathology; Mutation; Myosin Heavy Chains/genetics; Purpura, Thrombocytopenic, Idiopathic/complications; Thrombocytopenia/congenital; Child; Female; Hearing Loss, Sensorineural/etiology; Hearing Loss, Sensorineural/metabolism; Humans; Prognosis; Thrombocytopenia/etiology; Thrombocytopenia/metabolism; Thrombocytopenia/pathology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Thrombocytopenia / Purpura, Thrombocytopenic, Idiopathic / Myosin Heavy Chains / Hearing Loss, Sensorineural / Mutation Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Child / Female / Humans Language: En Journal: J Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2021 Type: Article

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