Thalassemia and pregnancy complications

نویسندگان

چکیده

Thalassemia is a blood disorder passed down through families (inherited) in which the body makes an abnormal form or inadequate amount of hemoglobin. Hemoglobin protein red cells that carries oxygen. The results large numbers being destroyed, leads to anemia. This alpha- beta-chain ratio causes unpaired chains precipitate and destruction cell precursors bone marrow (ineffective erythropoiesis) circulation (hemolysis). Affected individuals with thalassemia have variable degrees anemia extramedullary hematopoiesis, turn can cause changes, impaired growth, iron overload. Recurrent pregnancy loss (RPL), also known as recurrent miscarriages, defined by consecutive two more pregnancies same partner having no than one living child. Objective current review was determine maternal fetal outcomes women complicated .Conclusion: There are many changes complications stress make symptoms worse . should be considered high risk always preceded complete preconception assessment.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Survival and complications in thalassemia.

The life expectancy of patients with thalassemia major has significantly increased in recent years, as reported by several groups in different countries. However, complications are still frequent and affect the patients' quality of life. In a recent study from the United Kingdom, it was found that 50% of the patients had died before age 35. At that age, 65% of the patients from an Italian long-...

متن کامل

Neurological complications in b-thalassemia

Over the years, several reports have demonstrated involvement of the nervous system in b-thalassemia patients. Neurological complications have been attributed to various factors such as chronic hypoxia, bone marrow expansion, iron overload, and desferrioxamine neurotoxicity. In most cases, neurological involvement does not initially present with relevant signs or symptoms (i.e., is subclinical)...

متن کامل

Update on thalassemia: clinical care and complications.

beta-Thalassemia, originally named Cooley anemia, is an inherited blood disease. Various types of thalassemia are inherited anemias caused by mutations at the globin gene loci on chromosomes 16 and 11, affecting the production of alpha- or beta-globin protein, respectively. The combination of early diagnosis, improvements in monitoring for organ complications, and advances in supportive care ha...

متن کامل

Visual and Auditory Complications during Deferasirox Therapy in Beta-thalassemia

Background:  Deferasirox is an oral iron chelator widely used to treat iron overload in patients with transfusion-dependent β-thalassemia. This study investigated the prevalence of visual and auditory complications caused by deferasirox. Materials and Methods: This cross-sectional study included 156 patients aged less than 18 years with transfusion-dependent β-thalassemia and deferasirox iron...

متن کامل

major thalassemia and pregnancy

normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 β-thalassemia (cooley anemia) initially was described by dr cooley. [1] it is recognized that various types of thalassemia are inherited anemia caused by mutations at the globin gene, affecting the production of é‘ - or β-globin protein. the anemia interferes with red cell maturation. [2] β-globin gene mutations give rise ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: World Journal Of Advanced Research and Reviews

سال: 2022

ISSN: ['2581-9615']

DOI: https://doi.org/10.30574/wjarr.2022.14.1.0284