Abstract

Editorial1 October 1954HEREDITARY HEMOGLOBINOPATHIESMILTON S. SACKS, M.D.MILTON S. SACKS, M.D.Search for more papers by this authorAuthor, Article, and Disclosure Informationhttps://doi.org/10.7326/0003-4819-41-4-849 SectionsAboutPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinkedInRedditEmail ExcerptIn 1923 Taliaferro and Huck1proposed the theory that sickle cell disease, first described by Herrick2in 1910, was due to the inheritance of an abnormal gene which behaved as a Mendelian dominant characteristic. Clinical variation in severity, characterized as sicklemia (sickle cell trait) and sickle cell anemia respectively, was believed due to a difference in penetrance or expression of the abnormal gene. In vitro demonstration of sickling by exposure of erythrocytes to reduced oxygen tension, does not permit differentiation of the two clinical states. In 1940 Sherman3noted that a considerably greater reduction in oxygen tension was required to...1 TaliaferroHuck WHJG: The inheritance of sickle cell anemia in man, Genetics 8: 594, 1923. CrossrefMedlineGoogle Scholar2 Herrick JB: Peculiar elongated and sickle-shaped red corpuscles in a case of severe anemia, Arch. Int. Med. 6: 517, 1910. CrossrefGoogle Scholar3 Sherman IJ: The sickling phenomenon with special reference to the differentiation of sickle cell anemia from the sickle cell trait, Bull. Johns Hopkins Hosp. 67: 309, 1940. Google Scholar4 Neel JV: The inheritance of sickle cell anemia, Science 110: 64, 1949. CrossrefMedlineGoogle Scholar5 PaulingItanoSingerWells LHASJIC: Sickle cell anemia, a molecular disease, Science 110: 543, 1949. CrossrefMedlineGoogle Scholar6 Motulsky AG: A study of hereditary hemoglobinopathies, Clin. Research Proc. 2: 137, 1954. Google Scholar7 BeavenHochHoliday GHHER: The hemoglobins of the human fetus and infant. Electrophoretic and spectroscopic differentiation of adult and fetal types, Biochem. J. 49: 374, 1951. CrossrefMedlineGoogle Scholar8 SingerChernoffSinger KAIL: Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation, Blood 6: 413, 1951. CrossrefMedlineGoogle Scholar9 Liquori AM: Presence of fetal hemoglobin in Cooley's anemia, Nature 167: 950, 1951. CrossrefMedlineGoogle Scholar10 Rich A: Studies on the hemoglobin of Cooley's anemia and Cooley's trait, Proc. Nat. Acad. Sc. 38: 187, 1952. CrossrefMedlineGoogle Scholar11 WellsItano ICHA: Ratio of sickle cell anemia hemoglobin to normal hemoglobin in sicklemics, J. Biol. Chem. 188: 65, 1951. CrossrefMedlineGoogle Scholar12 Itano HA: Qualitative and quantitative control of adult hemoglobin synthesis. A multiple allele hypothesis, Am. J. Hum. Genet. 5: 34, 1953. MedlineGoogle Scholar13 ItanoNeel HAJV: A new inherited abnormality of human hemoglobin, Proc. Nat. Acad. Sc. 36: 613, 1951. CrossrefGoogle Scholar14 Statement concerning a system of nomenclature for the varieties of human hemoglobin, Blood 8: 386, 1953. MedlineGoogle Scholar15 Itano HA: A third abnormal hemoglobin associated with hereditary hemolytic anemia, Proc. Nat. Acad. Sc. 37: 775, 1951. CrossrefMedlineGoogle Scholar16 SilvestroniBianco EI: Micro-drepanocito-anemia in un soggetto di razza bianco, Boll. Atti. Accad. Med. Roma 70: 347, 1945. Google Scholar17 NeelItanoLawrence JVHAJS: Two cases of sickle cell disease presumably due to the combination of the genes for thalassemia and sickle cell hemoglobin, Blood 8: 434, 1953. CrossrefMedlineGoogle Scholar18 Durrum EL: A microelectrophoretic and microiontophoretic technique, J. Am. Chem. Soc. 72: 2943, 1950. CrossrefGoogle Scholar19 KunkelTiselius HGA: Electrophoresis of proteins on filter paper, J. Gen. Physiol. 35: 89, 1952. CrossrefGoogle Scholar20 Spaet TH: Identification of abnormal hemoglobins by means of paper electrophoresis, J. Lab. and Clin. Med. 41: 161, 1953. MedlineGoogle Scholar21 SmithConley EWCL: Filter paper electrophoresis of human hemoglobins with special reference to the incidence and clinical significance of hemoglobin C, Bull. Johns Hopkins Hosp. 93: 94, 1953. MedlineGoogle Scholar22 Neel JV: Implications of some recent developments in hematological and serological genetics, Am. J. Hum. Genet. 6: 208, 1954. MedlineGoogle Scholar23 NeelKaplanZullzer JVEWW: Further studies on hemoglobin C. Parts I and II, Blood 8: 724 and 735, 1953. CrossrefMedlineGoogle Scholar24 RanneyLarsonMcCormack HMDMGH: Some clinical, biochemical, and genetic observations on hemoglobin C, J. Clin. Invest. 32: 1277, 1953. CrossrefMedlineGoogle Scholar25 LevinSchneiderCuddJohnson WCRGJAJE: A family with homozygous hemoglobin C and sickle cell trait union: a clinical, hematological, and electrophoretic study, J. Lab. and Clin. Med. 42: 918, 1953. Google Scholar26 SpaetAlwayWard TARHG: Homozygous type C hemoglobin, Pediatrics 12: 483, 1953. MedlineGoogle Scholar27 MinnichNa-NakornChongchareonsukKochaseni VSSS: Mediterranean anemia. A study of 32 cases in Thailand, Blood 9: 1, 1954. CrossrefMedlineGoogle Scholar28 ChoremisIkinLehmannMourantZannos CEWHAEL: Sickle cell trait and blood groups in Greece, Lancet 2: 909, 1953. CrossrefGoogle Scholar29 LehmannCutbush AM: Sickle cell trait in southern India, Brit. M. J. 1: 404, 1952. CrossrefMedlineGoogle Scholar This content is PDF only. To continue reading please click on the PDF icon. Author, Article, and Disclosure InformationAuthors: MILTON S. SACKS, M.D.Affiliations: PreviousarticleNextarticle Advertisement FiguresReferencesRelatedDetails Metrics Cited byTHE GENETICS OF HUMAN HAEMOGLOBIN DIFFERENCES: PROBLEMS and PERSPECTIVES 1 October 1954Volume 41, Issue 4Page: 849-854KeywordsAnemiaHemoglobinopathiesOxygenSickle cell disease ePublished: 1 December 2008 Issue Published: 1 October 1954 PDF downloadLoading ...

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