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Profile of cystic fibrosis in a single referral center in Egypt
It was generally believed that Cystic fibrosis (CF) is rare among Arabs; however, the few studies available from Egypt and other Arabic countries suggested the presence of many undiagnosed patients. The aim of the present study was to determine the frequency of CF patients out of the referred cases...
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Published in: | Journal of advanced research 2014-09, Vol.5 (5), p.563-568 |
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description | It was generally believed that Cystic fibrosis (CF) is rare among Arabs; however, the few studies available from Egypt and other Arabic countries suggested the presence of many undiagnosed patients. The aim of the present study was to determine the frequency of CF patients out of the referred cases in a single referral hospital in Egypt. A total of 100 patients clinically suspected of having CF were recruited from the CF clinic of the Allergy and Pulmonology Unit, Children’s Hospital, Cairo University, Egypt, throughout a 2year period. Sweat chloride testing was done for all patients using the Wescor macroduct system for collection of sweat. Quantitative analysis for chloride was then done by the thiocyanate colorimetric method. Patients positive for sweat chloride (⩾60mmol/L) were tested for the ΔF508 mutation using primer specific PCR for cystic fibrosis transmembrane conductance regulator (CFTR) gene. Thirty-six patients (36%) had a positive sweat chloride test. The main clinical presentations in patients were chronic cough in 32 (88.9%), failure to thrive in 27 (75%), steatorrhea in 24 (66.7%), and hepatobiliary involvement in 5 (13.9%). Positive consanguinity was reported in 50% of CF patients. Thirty-two patients were screened for ΔF508 mutation. Positive ΔF508 mutation was detected in 22 (68.8%) patients, 8 (25%) were homozygous, 14 (43.8%) were heterozygous, and 10 (31.3%) tested were negative. CF was diagnosed in more than third of patients suspected of having the disease on clinical grounds. This high frequency of CF among referred patients indicates that a high index of suspicion and an increasing availability of diagnostic tests lead to the identification of a higher number of affected individuals. |
doi_str_mv | 10.1016/j.jare.2013.07.005 |
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The aim of the present study was to determine the frequency of CF patients out of the referred cases in a single referral hospital in Egypt. A total of 100 patients clinically suspected of having CF were recruited from the CF clinic of the Allergy and Pulmonology Unit, Children’s Hospital, Cairo University, Egypt, throughout a 2year period. Sweat chloride testing was done for all patients using the Wescor macroduct system for collection of sweat. Quantitative analysis for chloride was then done by the thiocyanate colorimetric method. Patients positive for sweat chloride (⩾60mmol/L) were tested for the ΔF508 mutation using primer specific PCR for cystic fibrosis transmembrane conductance regulator (CFTR) gene. Thirty-six patients (36%) had a positive sweat chloride test. The main clinical presentations in patients were chronic cough in 32 (88.9%), failure to thrive in 27 (75%), steatorrhea in 24 (66.7%), and hepatobiliary involvement in 5 (13.9%). Positive consanguinity was reported in 50% of CF patients. Thirty-two patients were screened for ΔF508 mutation. Positive ΔF508 mutation was detected in 22 (68.8%) patients, 8 (25%) were homozygous, 14 (43.8%) were heterozygous, and 10 (31.3%) tested were negative. CF was diagnosed in more than third of patients suspected of having the disease on clinical grounds. This high frequency of CF among referred patients indicates that a high index of suspicion and an increasing availability of diagnostic tests lead to the identification of a higher number of affected individuals.</description><identifier>ISSN: 2090-1232</identifier><identifier>EISSN: 2090-1224</identifier><identifier>DOI: 10.1016/j.jare.2013.07.005</identifier><identifier>PMID: 25685524</identifier><language>eng</language><publisher>Egypt: Elsevier B.V</publisher><subject>Children ; Egypt ; Original ; Sweat chloride ; ΔF508 mutation</subject><ispartof>Journal of advanced research, 2014-09, Vol.5 (5), p.563-568</ispartof><rights>2013</rights><rights>2013 Production and hosting by Elsevier B.V. on behalf of Cairo University. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c488t-4a182689df207f472c0e9f54b0fb8fdd3c9d1d21050bf15ee882b1c065ee6b083</citedby><cites>FETCH-LOGICAL-c488t-4a182689df207f472c0e9f54b0fb8fdd3c9d1d21050bf15ee882b1c065ee6b083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294314/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S2090123213000957$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,3535,27903,27904,45759,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25685524$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>El-Falaki, Mona M.</creatorcontrib><creatorcontrib>Shahin, Walaa A.</creatorcontrib><creatorcontrib>El-Basha, Noussa R.</creatorcontrib><creatorcontrib>Ali, Aliaa A.</creatorcontrib><creatorcontrib>Mehaney, Dina A.</creatorcontrib><creatorcontrib>El-Attar, Mona M.</creatorcontrib><title>Profile of cystic fibrosis in a single referral center in Egypt</title><title>Journal of advanced research</title><addtitle>J Adv Res</addtitle><description>It was generally believed that Cystic fibrosis (CF) is rare among Arabs; however, the few studies available from Egypt and other Arabic countries suggested the presence of many undiagnosed patients. The aim of the present study was to determine the frequency of CF patients out of the referred cases in a single referral hospital in Egypt. A total of 100 patients clinically suspected of having CF were recruited from the CF clinic of the Allergy and Pulmonology Unit, Children’s Hospital, Cairo University, Egypt, throughout a 2year period. Sweat chloride testing was done for all patients using the Wescor macroduct system for collection of sweat. Quantitative analysis for chloride was then done by the thiocyanate colorimetric method. Patients positive for sweat chloride (⩾60mmol/L) were tested for the ΔF508 mutation using primer specific PCR for cystic fibrosis transmembrane conductance regulator (CFTR) gene. Thirty-six patients (36%) had a positive sweat chloride test. The main clinical presentations in patients were chronic cough in 32 (88.9%), failure to thrive in 27 (75%), steatorrhea in 24 (66.7%), and hepatobiliary involvement in 5 (13.9%). Positive consanguinity was reported in 50% of CF patients. Thirty-two patients were screened for ΔF508 mutation. Positive ΔF508 mutation was detected in 22 (68.8%) patients, 8 (25%) were homozygous, 14 (43.8%) were heterozygous, and 10 (31.3%) tested were negative. CF was diagnosed in more than third of patients suspected of having the disease on clinical grounds. This high frequency of CF among referred patients indicates that a high index of suspicion and an increasing availability of diagnostic tests lead to the identification of a higher number of affected individuals.</description><subject>Children</subject><subject>Egypt</subject><subject>Original</subject><subject>Sweat chloride</subject><subject>ΔF508 mutation</subject><issn>2090-1232</issn><issn>2090-1224</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kF9LwzAUxYMobsx9AR-kj76s3qRJm4IoMuYfGOiDPoc2vZkZXTuTbrBvb8rm0Bfzkgvn3JOTHyGXFGIKNL1ZxsvCYcyAJjFkMYA4IUMGOUwoY_z0OCdsQMbeLyGcRMqc0nMyYCKVQjA-JPdvrjW2xqg1kd75zurI2NK13vrINlERedssguzQoHNFHWlsOnS9Nlvs1t0FOTNF7XF8uEfk43H2Pn2ezF-fXqYP84nmUnYTXlDJUplXhkFmeMY0YG4EL8GU0lRVovOKVoyCgNJQgSglK6mGNIxpCTIZkbt97npTrrDqW4Q2au3sqnA71RZW_VUa-6kW7VZxlvOE8hBwfQhw7dcGfadW1mus66LBduMVTYXIEgqJCFa2t-rAwYefH5-hoHr4aql6-KqHryBTAX5Yuvpd8LjygzoYbvcGDJi2Fp3y2mKjsbIOdaeq1v6X_w0rCpXR</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>El-Falaki, Mona M.</creator><creator>Shahin, Walaa A.</creator><creator>El-Basha, Noussa R.</creator><creator>Ali, Aliaa A.</creator><creator>Mehaney, Dina A.</creator><creator>El-Attar, Mona M.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140901</creationdate><title>Profile of cystic fibrosis in a single referral center in Egypt</title><author>El-Falaki, Mona M. ; Shahin, Walaa A. ; El-Basha, Noussa R. ; Ali, Aliaa A. ; Mehaney, Dina A. ; El-Attar, Mona M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-4a182689df207f472c0e9f54b0fb8fdd3c9d1d21050bf15ee882b1c065ee6b083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Children</topic><topic>Egypt</topic><topic>Original</topic><topic>Sweat chloride</topic><topic>ΔF508 mutation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>El-Falaki, Mona M.</creatorcontrib><creatorcontrib>Shahin, Walaa A.</creatorcontrib><creatorcontrib>El-Basha, Noussa R.</creatorcontrib><creatorcontrib>Ali, Aliaa A.</creatorcontrib><creatorcontrib>Mehaney, Dina A.</creatorcontrib><creatorcontrib>El-Attar, Mona M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of advanced research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>El-Falaki, Mona M.</au><au>Shahin, Walaa A.</au><au>El-Basha, Noussa R.</au><au>Ali, Aliaa A.</au><au>Mehaney, Dina A.</au><au>El-Attar, Mona M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Profile of cystic fibrosis in a single referral center in Egypt</atitle><jtitle>Journal of advanced research</jtitle><addtitle>J Adv Res</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>5</volume><issue>5</issue><spage>563</spage><epage>568</epage><pages>563-568</pages><issn>2090-1232</issn><eissn>2090-1224</eissn><abstract>It was generally believed that Cystic fibrosis (CF) is rare among Arabs; however, the few studies available from Egypt and other Arabic countries suggested the presence of many undiagnosed patients. 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Positive consanguinity was reported in 50% of CF patients. Thirty-two patients were screened for ΔF508 mutation. Positive ΔF508 mutation was detected in 22 (68.8%) patients, 8 (25%) were homozygous, 14 (43.8%) were heterozygous, and 10 (31.3%) tested were negative. CF was diagnosed in more than third of patients suspected of having the disease on clinical grounds. This high frequency of CF among referred patients indicates that a high index of suspicion and an increasing availability of diagnostic tests lead to the identification of a higher number of affected individuals.</abstract><cop>Egypt</cop><pub>Elsevier B.V</pub><pmid>25685524</pmid><doi>10.1016/j.jare.2013.07.005</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Children Egypt Original Sweat chloride ΔF508 mutation |
title | Profile of cystic fibrosis in a single referral center in Egypt |
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