Literature DB >> 2658854

Gall stones in Jamaican children with homozygous sickle cell disease.

D K Webb1, J S Darby, D T Dunn, S I Terry, G R Serjeant.   

Abstract

Gall stones were detected by ultrasonography in 30 of 226 (13%) children with homozygous sickle cell disease aged 5-13 years participating in a cohort study from birth. Children with gall stones had significantly lower total haemoglobin and fetal haemoglobin and higher bilirubin concentrations, but further analysis showed that the apparent effects of haemoglobin and fetal haemoglobin concentration were secondary to their relationship with bilirubin concentrations. Abdominal pain crises were significantly associated with gall stones but both factors appeared to reflect an increased clinical severity and were probably not causally related. No patients had symptoms specific of gall stones and an association with abdominal pain crisis should not, of itself, be considered an indication for surgery.

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Year:  1989        PMID: 2658854      PMCID: PMC1792039          DOI: 10.1136/adc.64.5.693

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  17 in total

1.  Screening cord bloods for detection of sickle cell disease in Jamaica.

Authors:  B E Serjeant; M Forbes; L L Williams; G R Serjeant
Journal:  Clin Chem       Date:  1974-06       Impact factor: 8.327

2.  Cholecystitis and cholelithiasis masking as abdominal crises in sickle cell disease.

Authors:  S Ariyan; F S Shessel; L K Pickett
Journal:  Pediatrics       Date:  1976-08       Impact factor: 7.124

3.  Cholelithiasis and biliary tract disease in sickle-cell disease in Nigerians.

Authors:  O Akinyanju; F Ladapo
Journal:  Postgrad Med J       Date:  1979-06       Impact factor: 2.401

4.  Cholelithiasis in sickle cell anemia: a case for elective cholecystectomy.

Authors:  D L Solanki; P R McCurdy
Journal:  Am J Med Sci       Date:  1979 May-Jun       Impact factor: 2.378

5.  Incidence of cholelithiasis in sickle cell anemia using the ultrasonic gray-scale technique.

Authors:  S Sarnaik; T L Slovis; D P Corbett; A Emami; C F Whitten
Journal:  J Pediatr       Date:  1980-06       Impact factor: 4.406

6.  The prevalence of cholelithiasis in sickle cell disease as diagnosed by ultrasound and cholecystography.

Authors:  B S Lachman; J Lazerson; R J Starshak; F M Vaughters; S L Werlin
Journal:  Pediatrics       Date:  1979-11       Impact factor: 7.124

7.  The development of haematological changes in homozygous sickle cell disease: a cohort study from birth to 6 years.

Authors:  G R Serjeant; Y Grandison; Y Lowrie; K Mason; J Phillips; B E Serjeant; S Vaidya
Journal:  Br J Haematol       Date:  1981-08       Impact factor: 6.998

8.  Cholelithiasis in children with sickle cell disease.

Authors:  G Karayalcin; N Hassani; M Abrams; P Lanzkowsky
Journal:  Am J Dis Child       Date:  1979-03

9.  Cholecystosonography in children with sickle cell disease: technical approach and clinical results.

Authors:  J J Cunningham; S M Houlihan; C Altay
Journal:  J Clin Ultrasound       Date:  1981 May-Jun       Impact factor: 0.910

10.  Cholelithiasis in sickle cell anemia: surgical or medical management.

Authors:  C G Stephens; R B Scott
Journal:  Arch Intern Med       Date:  1980-05
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  11 in total

Review 1.  Genetic modifiers of sickle cell disease.

Authors:  Martin H Steinberg; Paola Sebastiani
Journal:  Am J Hematol       Date:  2012-05-28       Impact factor: 10.047

2.  Laparoscopic cholecystectomy in adults with sickle cell disease.

Authors:  G Bonatsos; K Birbas; K Toutouzas; N Durakis
Journal:  Surg Endosc       Date:  2001-05-14       Impact factor: 4.584

3.  The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.

Authors:  Suad AlFadhli; Hassan Al-Jafer; Mays Hadi; Mashael Al-Mutairi; Rasheeba Nizam
Journal:  PLoS One       Date:  2013-10-30       Impact factor: 3.240

4.  Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up.

Authors:  B A I Attalla; Z A Karrar; G Ibnouf; A O Mohamed; O Abdelwahab; E M Nasir; M A El Seed
Journal:  Afr Health Sci       Date:  2013-03       Impact factor: 0.927

5.  Gall stones in homozygous sickle cell disease.

Authors:  D K Webb; D T Dunn; G R Serjeant
Journal:  Arch Dis Child       Date:  1989-09       Impact factor: 3.791

Review 6.  Intravascular hemolysis and the pathophysiology of sickle cell disease.

Authors:  Gregory J Kato; Martin H Steinberg; Mark T Gladwin
Journal:  J Clin Invest       Date:  2017-03-01       Impact factor: 14.808

7.  The pediatric hydroxyurea phase III clinical trial (BABY HUG): challenges of study design.

Authors:  Bruce W Thompson; Scott T Miller; Zora R Rogers; Renee C Rees; Russell E Ware; Myron A Waclawiw; Rathi V Iyer; James F Casella; Lori Luchtman-Jones; Sohail Rana; Courtney D Thornburg; Ram V Kalpatthi; Julio C Barredo; R Clark Brown; Sharada Sarnaik; Thomas H Howard; Lori Luck; Winfred C Wang
Journal:  Pediatr Blood Cancer       Date:  2010-02       Impact factor: 3.167

8.  Sonographic Diagnosis and Clinical Correlates of Gallbladder Stones in Patients with Sickle Cell Disease in Calabar, Nigeria.

Authors:  Grace B Inah; Emmanuel E Ekanem
Journal:  Open Access Maced J Med Sci       Date:  2019-01-12

9.  Cholelithiasis in patients with paediatric sickle cell anaemia in a Saudi hospital.

Authors:  Zakaria M Alhawsawi; Amna M Alshenqeti; Amal M Alqarafi; Leema K Alhussayen; Waheed A Turkistani
Journal:  J Taibah Univ Med Sci       Date:  2019-04-02

10.  [Digestives diseases associated to sickle cell anemia in Lubumbashi: epidemiological and clinical aspects].

Authors:  Manix Ilunga Banza; Jules Panda Mulefu; Lire Ipani Lire; Yannick Tietie Ben N'dwala; Israel Badypwyla Tshiamala; Vincent de Paul Kaoma Cabala
Journal:  Pan Afr Med J       Date:  2019-07-26
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