Transient neonatal cyanosis associated with a new Hb F variant: Hb F viseu

Journal of Pediatric Hematology/Oncology

Volumn 35, Issue 2, 2013, Pages

  Bento, Celeste ^a   Magalhães Maia, Tabita ^a   Carvalhais, Ines ^a   Moita, Filipa ^a   Abreu, Gabriela ^a   Relvas, Luis ^a   Pereira, Alexandra ^a   Farela Neves, José ^a   Ribeiro, Maria L ^a  

^a CENTRO HOSPITALAR E UNIVERSITÁRIO DE COIMBRA   (Portugal)

Author keywords

M hemoglobin; methemoglobinemia; neonatal cyanosis

Indexed keywords

GENOMIC DNA; HEMOGLOBIN GAMMA CHAIN; METHEMOGLOBIN; OXYGEN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CYANOSIS; DISEASE ASSOCIATION; DNA POLYMORPHISM; GENE; HBG2 GENE; HETEROZYGOSITY; HUMAN; MALE; METHEMOGLOBINEMIA; MISSENSE MUTATION; NEWBORN; NEWBORN CYANOSIS; OXYGEN SATURATION; OXYGEN THERAPY; PLACENTA INSUFFICIENCY; POSITIVE END EXPIRATORY PRESSURE; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; TACHYPNEA; TREATMENT FAILURE;

CYANOSIS; FETAL HEMOGLOBIN; HEMOGLOBIN M; HEMOGLOBINS, ABNORMAL; HUMANS; INFANT, NEWBORN; MALE; METHEMOGLOBIN;

EID: 84874489572     PISSN: 10774114     EISSN: 15363678     Source Type: Journal    
DOI: 10.1097/MPH.0b013e3182667be3     Document Type: Article

References (17)

1. Alarcon P, Werner E. Neonatal Hematology. Cambridge, UK: Cambridge University Press; 2005:155-158.
2. Kohli-Kumar M, Zwerdling T, Rucknagel DL. Hemoglobin F-Cincinnati, alpha 2G gamma 2 41(C7) Phe-Ser in a newborn with cyanosis. Am J Hematol. 1995;49:43-47.
3. Urabe D, Li W, Hattori Y, et al. A new case of Hb F-M-Osaka [G gamma 63(E7)His-Tyr] showed only benign neonatal cyanosis. Hemoglobin. 1996;20:169-173.
4. Dainer E, Shell R, Miller R, et al. Neonatal cyanosis due to a novel fetal hemoglobin: Hb F-Circleville [Ggamma63(E7)His-Leu, CAT>CTT]. Hemoglobin. 2008;32:596-600.
5. Crowley MA, Mollan TL, Abdulmalik OY, et al. A hemoglobin variant associated with neonatal cyanosis and anemia. N Engl J Med. 2011;364:1837-1843.
6. Priest JR, Watterson J, Jones RT, et al. Mutant fetal hemoglobin causing cyanosis in a newborn. Pediatrics. 1989; 83:734-736.
7. Molchanova TP, Wilson JB, Gu LH, et al. A second observation of the fetal methemoglobin variant Hb F-M-Fort Ripley or alpha 2G gamma 2(92)(F8)His-Tyr. Hemoglobin. 1992;16:389-398.
8. Percy MJ, McFerran NV, Lappin TRJ. Disorders of oxidised haemoglobin. Blood Rev. 2005;19:61-68.
9. Baraka AS, Ayoub CM, Yazbeck-Karam V, et al. Prophylactic methylene blue in a patient with congenital methemoglobine-mia. Can J Anesth. 2005;52:258-261.
10. Little PF, Williamson R, Annison G, et al. Polymorphisms of human g-globin genes in Mediterranean populations. Nature. 1979;282:316-318.
11. Wiedermann BF, Indrak K, Wilson JB, et al. Hb Saint Louis or alpha 2 beta 2(28)(B10)Leu-Gln in a Czechoslovakian male. Hemoglobin. 1986;10:673-676.
12. Hojas-Bernal R, McNab-Martin P, Fairbanks VF, et al. Hb Chile [beta28(B10)Leu-Met]: an unstable hemoglobin associated with chronic methemoglobinemia and sulfonamide or methylene blue-induced hemolytic anemia. Hemoglobin. 1999;23:125-134.
13. Miwa S. Significance of the determination of red cell enzyme activities. Am J Hematol. 1979;6:163-172.
14. Dacie JV, Lewis SM. Practical Haematology. Edinburgh, UK: Churchill Livingstone; 1995:210-212.
15. Venselaar H, Te Beek TA, Kuipers RK, et al. Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces. BMC Bioinfor-matics. 2010;11:548.
16. Thillet J, Cohen-Solal M, Seligmann M, et al. Functional and physicochemical studies of hemoglobin St. Louis beta 28 (B10) Leu replaced by Gln: a variant with ferric beta heme iron. J Clin Invest. 1976;58:1098-1106.
17. Ostrander RJ, Green NS. Neonatal cyanosis from a hemoglobin variant. N Engl J Med. 2011;365:378.