Serum and Red Cell Enzyme Variants in an Amerindian Tribe

1976 ◽  
Vol 26 (4) ◽  
pp. 252-262 ◽  
Author(s):  
H. Vergnes ◽  
J.C. Quilici ◽  
M. Gherardi ◽  
G. Bejarano
Keyword(s):  
Red Cell ◽  
1979 ◽  
Vol 50 (2) ◽  
pp. 271-277 ◽  
Author(s):  
H. W. Goedde ◽  
H. G. Benkmann ◽  
D. P. Agarwal ◽  
L. Hirth ◽  
U. Bienzle ◽  
...  

Nature ◽  
1969 ◽  
Vol 223 (5209) ◽  
pp. 892-892
Author(s):  
Keyword(s):  
Red Cell ◽  

2020 ◽  
pp. 5463-5472
Author(s):  
Alberto Zanella ◽  
Paola Bianchi

Numerous enzymes, including those of the hexose monophosphate and glycolytic pathways, are active in the red cell. They are required for the generation of ATP and the reductants NADH and NADPH. 2,3-Diphosphoglycerate, an intermediate of glucose metabolism, is a key regulator of the affinity of haemoglobin for oxygen, and accessory enzymes are also active for the synthesis of glutathione, disposal of oxygen free radicals, and for nucleotide metabolism. With the exception of heavy metal poisoning and rare cases of myelodysplasia, most red cell enzyme deficiency disorders are inherited. They may cause haematological abnormalities, (most commonly nonspherocytic haemolytic anaemias, but also rarely polycythaemia or methaemoglobinaemia, manifest with autosomal recessive or sex-linked inheritance), and may also be associated with nonhaematological disease when the defective enzyme is expressed throughout the body. Some may mirror important metabolic disorders, without producing haematological problems, making them of diagnostic value. Others are of no known clinical consequence. With rare exceptions, it is impossible to differentiate the enzymatic defects from one another by clinical or routine laboratory methods. Diagnosis depends on the combination of (1) accurate ascertainment of the family history; (2) morphological observations—these can determine whether haemolysis is present, rule out some causes of haemolysis (e.g. hereditary spherocytosis and other red blood cell membrane disorders), and diagnose pyrimidine 5′-nucleotidase deficiency (prominent red cell stippling); (3) estimation of red cell enzyme activity; and (4) molecular analysis. The most common red cell enzyme defects are glucose-6-phosphate dehydrogenase deficiency, pyruvate kinase deficiency, glucose-6-phosphate isomerase deficiency, pyrimidine 5′-nucleotidase deficiency—which may also induced by exposure to environmental lead—and triosephosphate isomerase deficiency.


1982 ◽  
Vol 32 (6) ◽  
pp. 385-403 ◽  
Author(s):  
P.B. Booth ◽  
D. Tills ◽  
A. Warlow ◽  
A.C. Kopeć ◽  
A.E. Mourant ◽  
...  

Blood ◽  
1977 ◽  
Vol 49 (6) ◽  
pp. 1022-1023 ◽  
Author(s):  
H Arnold ◽  
KG Blume ◽  
GW Lohr
Keyword(s):  
Red Cell ◽  

1977 ◽  
Vol 27 (6) ◽  
pp. 412-423 ◽  
Author(s):  
P.B. Booth ◽  
J.L. Faoagali ◽  
R.L. Kirk ◽  
N.M. Blake

2019 ◽  
Vol 72 (6) ◽  
pp. 393-398 ◽  
Author(s):  
Rashmi Dongerdiye ◽  
Pranoti Kamat ◽  
Punit Jain ◽  
Prashant Warang ◽  
Rati Devendra ◽  
...  

Adenylate kinase (AK) deficiency is a rare erythroenzymopathy associated with hereditary nonspherocytic haemolytic anaemia along with mental/psychomotor retardation in few cases. Diagnosis of AK deficiency depends on the decreased level of enzyme activity in red cell and identification of a mutation in the AK1 gene. Until, only eight mutations causing AK deficiency have been reported in the literature. We are reporting two novel missense mutation (c.71A > G and c.413G > A) detected in the AK1 gene by next-generation sequencing (NGS) in a 6-year-old male child from India. Red cell AK enzyme activity was found to be 30% normal. We have screened a total of 32 family members of the patient and showed reduced red cell enzyme activity and confirm mutations by Sanger’s sequencing. On the basis of Sanger sequencing, we suggest that the proband has inherited a mutation in AK1 gene exon 4 c.71A > G (p.Gln24Arg) from paternal family and exon 6 c.413G > A (p.Arg138His) from maternal family. Bioinformatics tools, such as SIFT, Polymorphism Phenotyping v.2, Mutation Taster, MutPred, also confirmed the deleterious effect of both the mutations. Molecular modelling suggests that the structural changes induced by p.Gln24Arg and p.Arg138His are pathogenic variants having a direct impact on the structural arrangement of the region close to the active site of the enzyme. In conclusion, NGS will be the best solution for diagnosis of very rare disorders leading to better management of the disease. This is the first report of the red cell AK deficiency from the Indian population.


Sign in / Sign up

Export Citation Format

Share Document