Literature DB >> 22755290

Report of haemoglobin J-Toronto and alpha thalassemia in a family from North of Iran.

Mohammad Reza Mahdavi1, Nooshin Bayat, Valeh Hadavi, Hosein Karami, Payam Roshan, Hossein Najmabadi, Hamed Rohanizadeh.   

Abstract

We report of an Iranian family with history of a rare haemoglobin variant, Haemoglobin J associated with alpha thalassemia, discovered while performing premarital thalassemia screening. In the present study we report the first case of haemoglobin J-Toronto [alpha 5 (A3) Ala > Asp] on -globin gene, found in a 16-year-old female from Mazandaran Province, North of Iran. Further investigation characterized the same mutation for mother and brother of the proband, whilst mother was also a carrier of an alpha thalassemia gene mutation (-alpha3.7). Haemoglobin J-Toronto was previously just reported from Canada and has not been found in any part of Iran.

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Year:  2012        PMID: 22755290

Source DB:  PubMed          Journal:  J Pak Med Assoc        ISSN: 0030-9982            Impact factor:   0.781


  1 in total

1.  Hemoglobin J in a patient with severe anemia, a case report from Nepal.

Authors:  Anish Kumar Shrestha; Ashes Rijal; Kapil Belbase; Anisha Shrestha; Sangam Shah; Sharmila Chaudhary; Simin Kunwar; Sant Kumar Yadav; Roman Dhital; Pawan Gyawali
Journal:  Ann Med Surg (Lond)       Date:  2022-09-15
  1 in total

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