A retrospective study on clinical manifestations of neonates with FXIII-A deficiency.

Naderi, Majid; Cohan, Nader; Shahramian, Iraj; Miri-Aliabad, Ghasem; Haghpanah, Sezaneh; Imani, Mahmood; Moghadam, Mohamad; Dehvari, Abdollah; Dorgalaleh, Akbar; Karimi, Mehran

Naderi, Majid; Cohan, Nader; Shahramian, Iraj; Miri-Aliabad, Ghasem; Haghpanah, Sezaneh; Imani, Mahmood; Moghadam, Mohamad; Dehvari, Abdollah; Dorgalaleh, Akbar; Karimi, Mehran.

Afiliação

Naderi M; Department of Pediatrics Hematology & Oncology, Ali Ebn-e Abitaleb Hospital Research Center For Children and Adolescents Health [RCCAH], Zahedan University of Medical Sciences, Zahedan, Iran.
Cohan N; Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Shahramian I; Pediatric Digestive and Hepatic Research Center, Zabol University of Medical Sciences, Zabol, Iran.
Miri-Aliabad G; Department of Pediatric, Zahedan University of Medical Sciences, Zahedan, Iran.
Haghpanah S; Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Imani M; Zahedan University of Medical Sciences, Zahedan, Iran.
Moghadam M; Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Dehvari A; Zahedan University of Medical Sciences, Zahedan, Iran.
Dorgalaleh A; Department of Hematology and Blood Transfusion, School of Allied Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Karimi M; Hematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: mkarimi820@gmail.com.

Blood Cells Mol Dis ; 77: 78-81, 2019 07.

Article em En | MEDLINE | ID: mdl-31005750

Assuntos

Deficiência do Fator XIII/diagnóstico; Doenças do Sistema Nervoso Central/diagnóstico; Doenças do Sistema Nervoso Central/etiologia; Estudos Transversais; Deficiência do Fator XIII/complicações; Feminino; Hemorragia/diagnóstico; Hemorragia/etiologia; Humanos; Recém-Nascido; Masculino; Fenótipo; Gravidez; Diagnóstico Pré-Natal; Estudos Retrospectivos; Fatores de Risco; Avaliação de Sintomas

Palavras-chave

Central nervous system bleeding; Clinical manifestations; FXIII deficiency; Neonates

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiência do Fator XIII Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Female / Humans / Male / Newborn / Pregnancy Idioma: En Ano de publicação: 2019 Tipo de documento: Article

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