Background Sickle cell disease was the first hemoglobinopathy to be linked to an inherited structural defect in the beta globin gene, and the first in which the point mutation resulting in the defect was identified and characterized. The scope of newborn screening for sickle cell disease, which began over 30 years ago, has evolved to include other hemoglobin diseases. Today, evaluation of newborns for hemoglobinopathies encompasses detection of point mutations which lead to structural defects in the alpha or beta globin chains (hemoglobinopathies) such as sickle cell disease, and detection of defects in rate of production of either alpha or beta globin chains (thalassemias). Taken together, the inherited disorders of hemoglobin are some the most common genetic disorders in the world. Because the different hemoglobin disorders coexist at a high frequency in many populations and because individuals may inherit more than one type, hemoglobin disorders present a complex series of clinical phenotypes.
Clinical In the newborn period, a transition occurs from primarily fetal hemoglobin (HbF) production to adult hemoglobin (HbA). This transition temporarily masks symptoms of disease. As a result, diseases associated with red blood cell sickling (Hb S, C, S/C,S/O, and S/D diseases) usually present during the first or second year of life, although milder cases may present much later. Usual presenting features are failure to thrive, repeated infection in infancy, painful dactylitis, and pallor. At this stage typical hematologic findings are established. Heterozygotes (e.g., Sickle cell trait ) are carriers with no clinical symptoms. Thalassemias present with a wide clinical diversity depending upon the degree to which the alpha or beta chains are being synthesized. In beta thalassemia major, or complete absence of beta chain production, newborns are asymptomatic. But as HbF declines, affected infants present with severe anemia (usually within the first two years). Beta thalassemia minor (partial synthesis) has a variable clinical course. In alpha thalassemia, absence of alpha chains is uniformly fatal to the newborn within days of birth, whereas partial production, as in hemoglobin H disease, may produce variable clinical symptoms.
Testing
Primary screening for hemoglobinopathies is by isoelectric focusing (IEF) of blood eluted from a dried blood spot. IEF separates the hemoglobins and identifies most common variants by band mobility. DNA probes which specifically identify HbS, HbC, HbE, HbO Arab and HbD are used to confirm abnormal findings by IEF. Reduced HbA and second tier DNA testing for common beta thalassemia mutations help to identify beta thalassemias. The presence of Hb Barts and/or Hb H in the IEF pattern detects alpha thalassemia.
Treatment
Apart from bone marrow transplantation, there is no curative treatment for hemoglobin disorders. Management for newborns affected with sickling diseases typically involves oral penicillin given daily and maintained throughout childhood, and vaccination against Pneumococcus, Meningococcus, and H influenzae. Because the diagnosis and therapy of this disorder is complex, the pediatrician is advised to manage the patient in close collaboration with a consulting pediatric hematology specialist.
Inheritance
Structurally abnormal hemoglobins follow autosomal recessive inheritance. Most abnormal hemoglobins cause little or no clinical manifestations in heterozygotes (one copy of the mutation), including Hb S, C, D, E, and O Arab. Because the production of alpha chains is controlled by four gene loci (two on each pair of chromosomes), each gene controls only about 25% of total alpha chain production, and hemoglobinopathies due to alpha chain abnormalities are uncommon compared to beta chain abnormalities.
References
Weatherall DJ, Clegg JB, Higgs DR and Wood WG. “The Hemoglobinopathies” in
The Metabolic and Molecular Bases of Inherited Disease, 8th edition, 2001. Scriver,
Beaudet, et al. McGraw-Hill, Vol III, Chapter 181, p. 4571-4626.
Web Sites
SaveBabies.org
Site established and maintained by parents of newborns affected with a rare genetic defect, with information for parents and professionals and links to other informative sites.
National Newborn Screening and Genetics Resource Center
Provides information and resources in the area of newborn screening and genetics to benefit health professionals, the public health community, consumers and government officials.
Disclaimers
The analyses conducted by PerkinElmer Genetics produce results that can be used by qualified physicians in the diagnosis of disorders described herein. Evidence of these conditions will be detected in the vast majority of affected individuals; however, due to genetic variability, age of the patient at the time of specimen collection, quality of the specimen, health status of the patient, and other variables, such conditions may not be detected in all affected patients. PerkinElmer Genetics makes no warranty whatsoever, express or implied, including any warranty as to accuracy, completeness or timeliness, concerning the information contained herein, and you should not assume that such information is complete or the most up-to-date information available. PerkinElmer Genetics shall not be liable for any loss, claim or damages caused in whole or in part by our provision of, or your use of, any of the information contained herein. As a general statement, this information was drawn from published literature and is not drawn from our patient population or screening experience. The information contained herein is not intended to be a substitute for professional medical advice and should not be used for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions.
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