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Quoted phrase not found in phrase index: "Hand-foot syndrome in sickle cell anemia"
Page 1
Clinical features of sickle cell anaemia in northern nigerian children.
Ambe JP, Mava Y, Chama R, Farouq G, Machoko Y. Ambe JP, et al. West Afr J Med. 2012 Apr-Jun;31(2):81-5. West Afr J Med. 2012. PMID: 23208475
Sickle cell anaemia survival to adulthood in Africa was reported to be 10-15% in the first decade of life, with the death rate of about 5% during subsequent decades. ...There were 333 case notes retrieved and reviewed with their age, sex, clinical features at …
Sickle cell anaemia survival to adulthood in Africa was reported to be 10-15% in the first decade of life, with the dea …
Sickle cell anemia- clinical manifestations in 100 patients and review of the literature.
Karayalcin G, Rosner F, Kim KY, Chandra P, Aballi AJ. Karayalcin G, et al. Am J Med Sci. 1975 Jan-Feb;269(1):51-68. doi: 10.1097/00000441-197501000-00007. Am J Med Sci. 1975. PMID: 1130436
The clinical and hematological features of 100 patients with sickle cell anemia are reviewed. The heart was enlarged and a murmur was heard in nearly 80 percent of patients. Pneumonia and pulmonary infarction occurred in 43 percent and 12 percent of patients, …
The clinical and hematological features of 100 patients with sickle cell anemia are reviewed. The heart was enlarged an …
The features of sickle cell disease in Saudi children.
el-Hazmi MA, Bahakim HM, al-Swailem AM, Warsy AS. el-Hazmi MA, et al. J Trop Pediatr. 1990 Aug;36(4):148-55. doi: 10.1093/tropej/36.4.148. J Trop Pediatr. 1990. PMID: 2213976
The patients with SCD were classified into five groups based on the absence of thalassaemia (sickle cell anaemia, SCA), presence of beta zero-thalassaemia (HbS/beta zero-thalassaemia), SCA with alpha-thalassaemia.2 [heterozygotes (-alpha/alpha alpha) or homoz …
The patients with SCD were classified into five groups based on the absence of thalassaemia (sickle cell anaemia, SCA), …
High rate of sickle cell anaemia in Sub-Saharan Africa underlines the need to screen all children with severe anaemia for the disease.
Kadima BT, Gini Ehungu JL, Ngiyulu RM, Ekulu PM, Aloni MN. Kadima BT, et al. Acta Paediatr. 2015 Dec;104(12):1269-73. doi: 10.1111/apa.13040. Epub 2015 Jun 4. Acta Paediatr. 2015. PMID: 25982693
AIM: Neonatal screening for sickle cell anaemia is not common practice in the Democratic Republic of Congo, and we determined the prevalence in children with unknown electrophoresis of haemoglobin and anaemia. ...Of these 807 children, 36 (4.5%) were homozygo …
AIM: Neonatal screening for sickle cell anaemia is not common practice in the Democratic Republic of Congo, and we dete …
On the nature of sickle cell disease in the south-western province of Saudi Arabia.
el-Hazmi MA, Warsy AS. el-Hazmi MA, et al. Acta Haematol. 1986;76(4):212-6. doi: 10.1159/000206058. Acta Haematol. 1986. PMID: 2437751
Sickle cell disease (SCD) occurs at a high prevalence in different parts of Saudi Arabia. ...Clinical examination revealed a severe disease with several cases suffering from the hand and foot syndrome....
Sickle cell disease (SCD) occurs at a high prevalence in different parts of Saudi Arabia. ...Clinical examination revealed a s …
Malaria, clinical features and acute crisis in children suffering from sickle cell disease in resource-limited settings: a retrospective description of 90 cases.
Aloni MN, Tshimanga BK, Ekulu PM, Ehungu JL, Ngiyulu RM. Aloni MN, et al. Pathog Glob Health. 2013 Jun;107(4):198-201. doi: 10.1179/2047773213Y.0000000089. Pathog Glob Health. 2013. PMID: 23816320 Free PMC article.
BACKGROUND: The prevalence of sickle cell disease (SCD) is extremely high in the Democratic Republic of Congo (DRC). ...Blackwater fever was a rare event. Hand-foot syndrome was present in 12.8% of patients, exclusively in those less than 5 year …
BACKGROUND: The prevalence of sickle cell disease (SCD) is extremely high in the Democratic Republic of Congo (DRC). ...Blackw …
Early onset dactylitis associated with the occurrence of severe events in children with sickle cell anaemia. The Paediatric Cohort of Guadeloupe (1984-99).
Foucan L, Ekouevi D, Etienne-Julan M, Salmi LR, Diara JP; Paediatric Cohort of Guadeloupe. Foucan L, et al. Paediatr Perinat Epidemiol. 2006 Jan;20(1):59-66. doi: 10.1111/j.1365-3016.2006.00692.x. Paediatr Perinat Epidemiol. 2006. PMID: 16420342
Dactylitis or hand-foot syndrome is related to intravascular sickling and classically occurs around 6 months of life when haemoglobin S levels reach pathological significance. ...The study period was 1 January 1984 to 31 December 1999. Medical data were recor …
Dactylitis or hand-foot syndrome is related to intravascular sickling and classically occurs around 6 months of life wh …
Routine hemoglobin electrophoresis for pediatric surgery day case in at-risk populations: Suggested algorithm for screening using clinical risk factors.
Ademuyiwa AO, Bode CO, Adekola OO, Desalu I, Elebute OA, Kushimo OT. Ademuyiwa AO, et al. Niger J Clin Pract. 2016 May-Jun;19(3):349-52. doi: 10.4103/1119-3077.179272. Niger J Clin Pract. 2016. PMID: 27022798
At least one parent of 78.2% knew their Hb phenotype, of which, 79% were HbAA. A history of jaundice (P = 0.0001), hand and foot syndrome (P = 0.0001), frontal bossing (P = 0.0001), and low packed cell volume at surgery (P = 0.001) were found significa …
At least one parent of 78.2% knew their Hb phenotype, of which, 79% were HbAA. A history of jaundice (P = 0.0001), hand and foot …
Observations on the natural history of dactylitis in homozygous sickle cell disease.
Stevens MC, Padwick M, Serjeant GR. Stevens MC, et al. Clin Pediatr (Phila). 1981 May;20(5):311-7. doi: 10.1177/000992288102000501. Clin Pediatr (Phila). 1981. PMID: 7226681
The incidence of the hand-foot syndrome (dactylitis) has been studied in a group of 233 children with homozygous sickle cell (SS) disease followed prospectively from birth. ...
The incidence of the hand-foot syndrome (dactylitis) has been studied in a group of 233 children with homozygous sic …
The haematological, biochemical and clinical--presentation of haemoglobin S in Saudi Arabia (i). Haematological & clinical expression.
El-Hazmi MA, Jabbar FA, Al-Faleh FZ, Al-Swailem AR, Warsy AS. El-Hazmi MA, et al. Trop Geogr Med. 1987 Apr;39(2):157-62. Trop Geogr Med. 1987. PMID: 3629709
The influence of alpha thalassaemia in each genotype was also investigated. The total haemoglobin concentration (Hb), red blood cell count (RBC) and packed cell volume (PCV) were significantly lower in the SS group without thalassaemia. ...The clinical investigation …
The influence of alpha thalassaemia in each genotype was also investigated. The total haemoglobin concentration (Hb), red blood cell …