Dermatoglyphic Patterns in Sickle Cell Anaemia Patients of Chhattisgarh, India
نویسندگان
چکیده
منابع مشابه
Incidence of Sickle Cell Anaemia and Thalassaemia in Central India
Haemoglobinopathies are group of diseases characterized by abnormalities both quantitative and qualitative in the synthesis of haemoglobin. Haemoglobinopathies consist of sickle cell anaemia (SCA), thalassaemia (β) and variant haemoglobins. In India, they are responsible for the largest number of genetic disorders and hence are of great public health hazardous. In India major concerned haemoglo...
متن کاملIron deficiency anaemia in sickle cell disorders in India.
BACKGROUND & OBJECTIVE Iron deficiency anaemia (IDA) is uncommon in individuals with sickle cell disease (SCD) because of availability of an adequate iron source potentially from increased red cell turnover and from blood transfusions. Also, iron deficiency anaemia can often go unnoticed because the sickle cell disease patients are already anaemic. Iron deficiency in sickle cell patients may re...
متن کاملAnaesthesia in Patients with Sickle-cell Anaemia.
Sir,—We were very interested to read Dr. R. A. Browne's article on this subject (Brit. J. Anaesth. (1965), 37, 181) and feel that a case which we were requested to anaesthetize might be worthy of comment in this connection. The patient was a West Indian woman, age 27 years, gravida-4 with a long history of sickle-cell anaemia, for which she had received alkalis plus blood transfusions. She was ...
متن کاملSickle Cell Disease and Sickle Cell Anaemia
Sickle cell haemoglobin (HbS) results from an autosomal recessively inherited mutation in which the 17th nucleotide of the beta globin gene is changed from thymine to adenine and the amino acid glutamic acid is replaced by valine at position 6 in the beta globin chain. [1, 2]Sickle cells have a reduced deformability and are easily destroyed, causing occlusion of the microcirculation and a chron...
متن کاملEffect of Lisinopril on Microalbuminuria in Sickle Cell Anaemia Children: A Single-Blind Randomized Controlled Trial
Background Sickle cell nephropathy is a major cause of morbidity and mortality in sickle cell anaemia (SCA). Proteinuria contributes to progression of renal damage. Icroalbuminuria is an early feature of SCN and progression to advanced kidney damage is delayed if regression is achieved with angiotensin converting enzyme inhibitors. We aimed to ...
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ژورنال
عنوان ژورنال: Open Access Journal of Dental Sciences
سال: 2017
ISSN: 2573-8771
DOI: 10.23880/oajds-16000141