Association of hemoglobinosis D-Punjab and β-thalassemia in a Moroccan family | Zendy

Mohamed Zaïd Saoud | Zendy; Asmâa Biaz | Zendy; Achraf Rachid | Zendy; Ghizlane El Amin | Zendy; Abdellah Dami | Zendy; Zohra Ouzzif | Zendy

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Association of hemoglobinosis D-Punjab and β-thalassemia in a Moroccan family

Author(s) -

Mohamed Zaïd Saoud,

Asmâa Biaz,

Achraf Rachid,

Ghizlane El Amin,

Abdellah Dami,

Zohra Ouzzif

Publication year - 2020

Publication title -

annales de biologie clinique

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.167

H-Index - 27

eISSN - 1950-6112

pISSN - 0003-3898

DOI - 10.1684/abc.2020.1523

Subject(s) - thalassemia , association (psychology) , medicine , beta thalassemia , genetics , traditional medicine , biology , psychology , psychotherapist

Hemoglobin D-Punjab is a common hemoglobin variant in India but very rare in Morocco. Often, its presence has minimal or no clinical impact. Its heterozygous association with β-thalassemia is exceptional. The purpose of the study is to describe the epidemiological, diagnostic and prophylactic aspects of hemoglobinosis D-Punjab from a family case study.

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