Hereditary Palmoplantar Keratodermas in South India
Thirty‐one patients with inherited palmoplantar keratodermas (PPKs) were screened from 59,490 cases who visiting the OPD of JIPMER, Pondicherry. The prevalence rate was 5.2 per 10,000 population (1:2000 approx.). PPKs were more common in males (25 patients) than females (6 patients); the overall mal...
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Veröffentlicht in: | Journal of dermatology 1997-12, Vol.24 (12), p.765-768 |
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description | Thirty‐one patients with inherited palmoplantar keratodermas (PPKs) were screened from 59,490 cases who visiting the OPD of JIPMER, Pondicherry. The prevalence rate was 5.2 per 10,000 population (1:2000 approx.). PPKs were more common in males (25 patients) than females (6 patients); the overall male to female ratio was 4.2:1. The incidence was highest in the group from 0–10 years of life (67.7% of cases). Unna‐Thost syndrome topped the list with 38.7% of cases and its prevalence 1:6000 (approx.), followed by Greither's disease (22.9%) and others‐Vohwinkel (3 cases), idiopathic punctate (2 cases), ichthyosis vulgaris associated PPK (2 cases) etc. This study has for the first time reported the prevalence and patterns of hereditary PPKs in South India. |
doi_str_mv | 10.1111/j.1346-8138.1997.tb02322.x |
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The prevalence rate was 5.2 per 10,000 population (1:2000 approx.). PPKs were more common in males (25 patients) than females (6 patients); the overall male to female ratio was 4.2:1. The incidence was highest in the group from 0–10 years of life (67.7% of cases). Unna‐Thost syndrome topped the list with 38.7% of cases and its prevalence 1:6000 (approx.), followed by Greither's disease (22.9%) and others‐Vohwinkel (3 cases), idiopathic punctate (2 cases), ichthyosis vulgaris associated PPK (2 cases) etc. This study has for the first time reported the prevalence and patterns of hereditary PPKs in South India.</description><identifier>ISSN: 0385-2407</identifier><identifier>EISSN: 1346-8138</identifier><identifier>DOI: 10.1111/j.1346-8138.1997.tb02322.x</identifier><identifier>PMID: 9492439</identifier><language>eng</language><publisher>England</publisher><subject>Adolescent ; Adult ; Age Distribution ; Child ; Child, Preschool ; Female ; hereditary ; Humans ; India - epidemiology ; Infant ; Keratoderma, Palmoplantar - epidemiology ; Keratoderma, Palmoplantar - genetics ; Male ; palmoplantar keratodermas ; Prevalence ; Risk Factors ; Sex Distribution</subject><ispartof>Journal of dermatology, 1997-12, Vol.24 (12), p.765-768</ispartof><rights>1997 Japanese Dermatological Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3152-67b005b785615cba628378839c4b0db765ead5edbe647035ea0ef3d5c26465963</citedby><cites>FETCH-LOGICAL-c3152-67b005b785615cba628378839c4b0db765ead5edbe647035ea0ef3d5c26465963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1346-8138.1997.tb02322.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1346-8138.1997.tb02322.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9492439$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gulati, Sanjeev</creatorcontrib><creatorcontrib>Thappa, Devinder Mohan</creatorcontrib><creatorcontrib>Garg, Bhagat Ram</creatorcontrib><title>Hereditary Palmoplantar Keratodermas in South India</title><title>Journal of dermatology</title><addtitle>J Dermatol</addtitle><description>Thirty‐one patients with inherited palmoplantar keratodermas (PPKs) were screened from 59,490 cases who visiting the OPD of JIPMER, Pondicherry. The prevalence rate was 5.2 per 10,000 population (1:2000 approx.). PPKs were more common in males (25 patients) than females (6 patients); the overall male to female ratio was 4.2:1. The incidence was highest in the group from 0–10 years of life (67.7% of cases). Unna‐Thost syndrome topped the list with 38.7% of cases and its prevalence 1:6000 (approx.), followed by Greither's disease (22.9%) and others‐Vohwinkel (3 cases), idiopathic punctate (2 cases), ichthyosis vulgaris associated PPK (2 cases) etc. This study has for the first time reported the prevalence and patterns of hereditary PPKs in South India.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Distribution</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>hereditary</subject><subject>Humans</subject><subject>India - epidemiology</subject><subject>Infant</subject><subject>Keratoderma, Palmoplantar - epidemiology</subject><subject>Keratoderma, Palmoplantar - genetics</subject><subject>Male</subject><subject>palmoplantar keratodermas</subject><subject>Prevalence</subject><subject>Risk Factors</subject><subject>Sex Distribution</subject><issn>0385-2407</issn><issn>1346-8138</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkMlOwzAQhi0EKqXwCEgRB24JXmI75gQqhRYqgQScLTt2RaosxU5E-_Y4NOqducyM_lk_AK4QTFCwm3WCSMriDJEsQULwpNUQE4yT7REYH6RjMIYkozFOIT8FZ96vIcSCIjgCI5EKnBIxBmRunTVFq9wuelNl1WxKVYcserFOtY2xrlI-Kurovenar2hRm0Kdg5OVKr29GPwEfD7OPqbzePn6tJjeL-OcIIpjxjWEVPOMMkRzrRjOCM8yIvJUQ6M5o1YZao22LOWQhAzaFTE0xyxlVDAyAdf7uRvXfHfWt7IqfG7LcKFtOi-5oBwjTkPh7b4wd433zq7kxhVVeEkiKHtici17LLLHInticiAmt6H5ctjS6cqaQ-uAKOh3e_2nKO3uH5Pl88PsLyS_JT96jw</recordid><startdate>199712</startdate><enddate>199712</enddate><creator>Gulati, Sanjeev</creator><creator>Thappa, Devinder Mohan</creator><creator>Garg, Bhagat Ram</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199712</creationdate><title>Hereditary Palmoplantar Keratodermas in South India</title><author>Gulati, Sanjeev ; Thappa, Devinder Mohan ; Garg, Bhagat Ram</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3152-67b005b785615cba628378839c4b0db765ead5edbe647035ea0ef3d5c26465963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Distribution</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>hereditary</topic><topic>Humans</topic><topic>India - epidemiology</topic><topic>Infant</topic><topic>Keratoderma, Palmoplantar - epidemiology</topic><topic>Keratoderma, Palmoplantar - genetics</topic><topic>Male</topic><topic>palmoplantar keratodermas</topic><topic>Prevalence</topic><topic>Risk Factors</topic><topic>Sex Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gulati, Sanjeev</creatorcontrib><creatorcontrib>Thappa, Devinder Mohan</creatorcontrib><creatorcontrib>Garg, Bhagat Ram</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gulati, Sanjeev</au><au>Thappa, Devinder Mohan</au><au>Garg, Bhagat Ram</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hereditary Palmoplantar Keratodermas in South India</atitle><jtitle>Journal of dermatology</jtitle><addtitle>J Dermatol</addtitle><date>1997-12</date><risdate>1997</risdate><volume>24</volume><issue>12</issue><spage>765</spage><epage>768</epage><pages>765-768</pages><issn>0385-2407</issn><eissn>1346-8138</eissn><abstract>Thirty‐one patients with inherited palmoplantar keratodermas (PPKs) were screened from 59,490 cases who visiting the OPD of JIPMER, Pondicherry. The prevalence rate was 5.2 per 10,000 population (1:2000 approx.). PPKs were more common in males (25 patients) than females (6 patients); the overall male to female ratio was 4.2:1. The incidence was highest in the group from 0–10 years of life (67.7% of cases). Unna‐Thost syndrome topped the list with 38.7% of cases and its prevalence 1:6000 (approx.), followed by Greither's disease (22.9%) and others‐Vohwinkel (3 cases), idiopathic punctate (2 cases), ichthyosis vulgaris associated PPK (2 cases) etc. This study has for the first time reported the prevalence and patterns of hereditary PPKs in South India.</abstract><cop>England</cop><pmid>9492439</pmid><doi>10.1111/j.1346-8138.1997.tb02322.x</doi><tpages>4</tpages></addata></record> |
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subjects | Adolescent Adult Age Distribution Child Child, Preschool Female hereditary Humans India - epidemiology Infant Keratoderma, Palmoplantar - epidemiology Keratoderma, Palmoplantar - genetics Male palmoplantar keratodermas Prevalence Risk Factors Sex Distribution |
title | Hereditary Palmoplantar Keratodermas in South India |
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