Literature DB >> 21854111

Leptin deficiency and leptin gene mutations in obese children from Pakistan.

Warda Fatima1, Adeela Shahid, Muhammad Imran, Jaida Manzoor, Shahida Hasnain, Sobia Rana, Saqib Mahmood.   

Abstract

BACKGROUND: Congenital leptin deficiency is a rare human genetic condition clinically characterized by hyperphagia and acute weight gain usually during the first postnatal year. The worldwide data on this disorder includes only 14 cases and four pathogenic mutations have been reported in the leptin gene. STUDY
OBJECTIVE: The objectives of this study were to measure serum leptin levels in obese children and to detect leptin gene mutations in those found to be leptin deficient. PATIENTS AND
RESULTS: A total of 25 obese children were recruited for the study. Leptin deficiency was detected in nine of them. Leptin gene sequencing identified mutations in homozygous state in all the leptin deficient children. Two cases carried novel mutations (c.481_482delCT and c.104_106delTCA) and each of the remaining seven the previously reported frameshift mutation (c.398delG).
CONCLUSION: The results suggest that leptin deficiency caused by mutations in the leptin gene may frequently be seen in obese Pakistani children from Central Punjab.

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Year:  2011        PMID: 21854111     DOI: 10.3109/17477166.2011.608431

Source DB:  PubMed          Journal:  Int J Pediatr Obes        ISSN: 1747-7166


  20 in total

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Review 5.  Chemical identity of hypothalamic neurons engaged by leptin in reproductive control.

Authors:  Dhirender V Ratra; Carol F Elias
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6.  A novel mutation in the leptin gene (W121X) in an Egyptian family.

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8.  Monogenic forms of childhood obesity due to mutations in the leptin gene.

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9.  The p. N103K mutation of leptin (LEP) gene and severe early onset obesity in Pakistan.

Authors:  Shahida Hasnain
Journal:  Biol Res       Date:  2016-04-13       Impact factor: 5.612

Review 10.  The Effects of Leptin Replacement on Neural Plasticity.

Authors:  Gilberto J Paz-Filho
Journal:  Neural Plast       Date:  2016-01-03       Impact factor: 3.599

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