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Information Journal Paper

Title

A Case Report of Hutchinson-Gilford Progeria Syndrome

Pages

  84-91

Abstract

 Hutchinson-Gilford Progeria Syndrome (HGPS), a rare genetic condition occurs one in every 8 million live births. HGPS is characterized by Premature aging in various organs. The average survival rate of the affected patients is 13 years, and their most common causes of death are myocardial infarction and stroke. This disease occurs due to a gene mutation in the chromosomes of the patient. There is no definitive treatment for Progeria, and most patients die at the age of 8 to 10 years. Scientists are interested in identifying this syndrome, as it may reveal the signs of a natural aging process at an early age. The studied patient was older than the global average with no cardiovascular disease and suffered from appendicitis.

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    APA: Copy

    YAGHOUBI, SIAMAK, Mohammadi, Sareh, YEKEFALLAH, LEILI, Taromiha, Alireza, & BAGHERI, AMENEH. (2019). A Case Report of Hutchinson-Gilford Progeria Syndrome. JOURNAL OF INFLAMMATORY DISEASES (THE JOURNAL OF QAZVIN UNIVERSITY OF MEDICAL SCIENCES), 23(1 (102) ), 84-91. SID. https://sid.ir/paper/49068/en

    Vancouver: Copy

    YAGHOUBI SIAMAK, Mohammadi Sareh, YEKEFALLAH LEILI, Taromiha Alireza, BAGHERI AMENEH. A Case Report of Hutchinson-Gilford Progeria Syndrome. JOURNAL OF INFLAMMATORY DISEASES (THE JOURNAL OF QAZVIN UNIVERSITY OF MEDICAL SCIENCES)[Internet]. 2019;23(1 (102) ):84-91. Available from: https://sid.ir/paper/49068/en

    IEEE: Copy

    SIAMAK YAGHOUBI, Sareh Mohammadi, LEILI YEKEFALLAH, Alireza Taromiha, and AMENEH BAGHERI, “A Case Report of Hutchinson-Gilford Progeria Syndrome,” JOURNAL OF INFLAMMATORY DISEASES (THE JOURNAL OF QAZVIN UNIVERSITY OF MEDICAL SCIENCES), vol. 23, no. 1 (102) , pp. 84–91, 2019, [Online]. Available: https://sid.ir/paper/49068/en

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