Literature DB >> 7868492

Sickle cell syndromes in and around Bardoli.

S R Iyer1, R R Iyer, G D Oza, R M Rane, R M Khandwala, P K Desai, S D Desai.   

Abstract

The study comprised of 2 groups. In group I sickling test was done in students studying in a school which mainly caters to the educational needs of the backward community. Out of 130 students examined 24 were found to be sicklers. The distribution of this cases among various castes/tribes were as follows--Choudharys (Cd)-13, Gamits (Gt)-4, Dhodhia Patels (DP)-4, Koknis (K)-2 and Koli Patel (KP)-1. In group II, patients admitted in the hospital between Jan '81 to June '82 were studied. The prevalence of sickle cell syndrome was 1.74%. The most common mode of presentation were limb pains and weakness. Hemoglobin values ranged from 3.0 gram% to 12 gms%. 35 cases of HbSS, 149 cases of HbAS and 1 case of Sickle Beta thalassemia were seen. The distribution of the cases amongst the various tribes and castes were as follows-Cd-93, Gt-56, DP-23, KP-7, K-4 and Rathods (R)-2. No cases were found in Anavil Brahmins or Patidar Patels. Clinical and pathological observations included palpable splenomegaly in 54 cases, splenic abscess in 1 case, isothenuria in large number of patients, microscopic hematuria in 6 cases and frank hematuria in 1 case. Osteomyelitis and cholecystitis were seen in one case each.

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Year:  1994        PMID: 7868492

Source DB:  PubMed          Journal:  J Assoc Physicians India        ISSN: 0004-5772


  2 in total

1.  Splenic Syndrome due to Sickle Cell Trait amongst Indian Soldiers Serving in Kashmir.

Authors:  M M Arora; J K Bhatia; V Khanna; P Jaiswal; V D Charan
Journal:  Med J Armed Forces India       Date:  2011-07-21

2.  Prevalence and hematological profile of β-thalassemia and sickle cell anemia in four communities of Surat city.

Authors:  Dipal S Bhukhanvala; Smita M Sorathiya; Avani P Shah; Ankur G Patel; Snehalata C Gupte
Journal:  Indian J Hum Genet       Date:  2012-05
  2 in total

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