An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.

Lee, Helena H L; Mak, Annisa S L; Kou, K O; Poon, C F; Wong, W S; Chiu, K H; Au, Patrick K C; Chan, Kelvin Y K; Kan, Anita S Y; Tang, Mary H Y; Leung, K Y

Lee, Helena H L; Mak, Annisa S L; Kou, K O; Poon, C F; Wong, W S; Chiu, K H; Au, Patrick K C; Chan, Kelvin Y K; Kan, Anita S Y; Tang, Mary H Y; Leung, K Y.

Afiliación

Lee HH; a Department of Obstetrics and Gynaecology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Mak AS; a Department of Obstetrics and Gynaecology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Kou KO; a Department of Obstetrics and Gynaecology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Poon CF; a Department of Obstetrics and Gynaecology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Wong WS; b Department of Clinical Pathology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Chiu KH; c Department of Paediatrics , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.
Au PK; d Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital , The University of Hong Kong , Hong Kong SAR , People's Republic of China.
Chan KY; d Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital , The University of Hong Kong , Hong Kong SAR , People's Republic of China.
Kan AS; d Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital , The University of Hong Kong , Hong Kong SAR , People's Republic of China.
Tang MH; d Prenatal Diagnostic Laboratory, Department of Obstetrics and Gynaecology, Tsan Yuk Hospital , The University of Hong Kong , Hong Kong SAR , People's Republic of China.
Leung KY; a Department of Obstetrics and Gynaecology , Queen Elizabeth Hospital , Hong Kong SAR , People's Republic of China.

Hemoglobin ; 40(6): 431-434, 2016 Nov.

Article en En | MEDLINE | ID: mdl-28361594

Asunto(s)

Anemia Diseritropoyética Congénita/diagnóstico; Anemia Diseritropoyética Congénita/genética; Heterocigoto; Hidropesía Fetal/genética; Factores de Transcripción de Tipo Kruppel/genética; Mutación; Adulto; Anemia Diseritropoyética Congénita/etiología; Anemia Diseritropoyética Congénita/terapia; Transfusión de Sangre Intrauterina; Examen de la Médula Ósea; Cordocentesis; Femenino; Humanos; Hidropesía Fetal/diagnóstico; Hidropesía Fetal/etiología; Hidropesía Fetal/terapia; Lactante; Masculino; Embarazo; Diagnóstico Prenatal

Palabras clave

Congenital dyserythropoietic anemia; Krüppel-like factor 1 (KLF1) gene mutations; fetal anemia; hydrops fetalis; intrauterine transfusion

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hidropesía Fetal / Factores de Transcripción de Tipo Kruppel / Heterocigoto / Anemia Diseritropoyética Congénita / Mutación Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Adult / Female / Humans / Infant / Male / Pregnancy Idioma: En Revista: Hemoglobin Año: 2016 Tipo del documento: Article

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