X-Linked reticulate pigmentary disorder in a female patient
Background X‐Linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex. Methods We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder. Results On examination, there were multiple, asymptomatic,...
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| Veröffentlicht in: | International journal of dermatology 2010-04, Vol.49 (4), p.421-425 |
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| container_title | International journal of dermatology |
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| creator | Kim, Byung Soo Seo, Sang-Hee Jung, Hong Dae Kwon, Kyung-Sool Kim, Moon-Bum |
| description | Background X‐Linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex.
Methods We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder.
Results On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed.
Conclusions Although a genetic study was not performed, we believe that our patient can be diagnosed with X‐linked reticulate pigmentary disorder according to the clinical and histopathologic findings. |
| doi_str_mv | 10.1111/j.1365-4632.2010.04102.x |
| format | Article |
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Methods We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder.
Results On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed.
Conclusions Although a genetic study was not performed, we believe that our patient can be diagnosed with X‐linked reticulate pigmentary disorder according to the clinical and histopathologic findings.</description><identifier>ISSN: 0011-9059</identifier><identifier>EISSN: 1365-4632</identifier><identifier>DOI: 10.1111/j.1365-4632.2010.04102.x</identifier><identifier>PMID: 20465698</identifier><identifier>CODEN: IJDEBB</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Biological and medical sciences ; Dermatology ; Female ; Genetic Diseases, X-Linked - diagnosis ; Genetic Diseases, X-Linked - pathology ; Humans ; Hyperpigmentation - diagnosis ; Hyperpigmentation - genetics ; Medical sciences ; Pigmentary diseases of the skin</subject><ispartof>International journal of dermatology, 2010-04, Vol.49 (4), p.421-425</ispartof><rights>2010 The International Society of Dermatology</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4362-2370562b9cc1eaa8d92b1919f7159dd79325b694836ca265e47e3255e2b7d7553</citedby><cites>FETCH-LOGICAL-c4362-2370562b9cc1eaa8d92b1919f7159dd79325b694836ca265e47e3255e2b7d7553</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.1365-4632.2010.04102.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-4632.2010.04102.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22526149$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20465698$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Byung Soo</creatorcontrib><creatorcontrib>Seo, Sang-Hee</creatorcontrib><creatorcontrib>Jung, Hong Dae</creatorcontrib><creatorcontrib>Kwon, Kyung-Sool</creatorcontrib><creatorcontrib>Kim, Moon-Bum</creatorcontrib><title>X-Linked reticulate pigmentary disorder in a female patient</title><title>International journal of dermatology</title><addtitle>Int J Dermatol</addtitle><description>Background X‐Linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex.
Methods We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder.
Results On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed.
Conclusions Although a genetic study was not performed, we believe that our patient can be diagnosed with X‐linked reticulate pigmentary disorder according to the clinical and histopathologic findings.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Dermatology</subject><subject>Female</subject><subject>Genetic Diseases, X-Linked - diagnosis</subject><subject>Genetic Diseases, X-Linked - pathology</subject><subject>Humans</subject><subject>Hyperpigmentation - diagnosis</subject><subject>Hyperpigmentation - genetics</subject><subject>Medical sciences</subject><subject>Pigmentary diseases of the skin</subject><issn>0011-9059</issn><issn>1365-4632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtv1DAURi0EosOUv4CyQawS_IjtWIgFGmAoCnTTAjvLcW6Qp3lM7URM_z1OM51u643te8_nx0EoITgjcbzfZYQJnuaC0YziWMU5wTQ7PEOrU-M5WmFMSKowV2foVQi7uGWU5C_RGcW54EIVK_ThT1q6_gbqxMPo7NSaEZK9-9tBPxp_l9QuDL4Gn7g-MUkDnWlj34wu9s_Ri8a0AV4f5zW6_vrlavMtLS-3F5tPZWpzJmhKmcRc0EpZS8CYola0IoqoRhKu6loqRnklVF4wYQ0VHHIJscSBVrKWnLM1erecu_fD7QRh1J0LFtrW9DBMQUvGOKUSi0gWC2n9EIKHRu-96-I_NMF6Nqd3ehakZ0F6NqfvzelDjL45XjJVHdSn4IOqCLw9AiZY0zbe9NaFR45yKkiuIvdx4f65Fu6e_AB98f3zvIr5dMm7MMLhlDf-RgvJJNe_f271L6x-lGzDdcn-A2KqlgE</recordid><startdate>201004</startdate><enddate>201004</enddate><creator>Kim, Byung Soo</creator><creator>Seo, Sang-Hee</creator><creator>Jung, Hong Dae</creator><creator>Kwon, Kyung-Sool</creator><creator>Kim, Moon-Bum</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><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>201004</creationdate><title>X-Linked reticulate pigmentary disorder in a female patient</title><author>Kim, Byung Soo ; Seo, Sang-Hee ; Jung, Hong Dae ; Kwon, Kyung-Sool ; Kim, Moon-Bum</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4362-2370562b9cc1eaa8d92b1919f7159dd79325b694836ca265e47e3255e2b7d7553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Dermatology</topic><topic>Female</topic><topic>Genetic Diseases, X-Linked - diagnosis</topic><topic>Genetic Diseases, X-Linked - pathology</topic><topic>Humans</topic><topic>Hyperpigmentation - diagnosis</topic><topic>Hyperpigmentation - genetics</topic><topic>Medical sciences</topic><topic>Pigmentary diseases of the skin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Byung Soo</creatorcontrib><creatorcontrib>Seo, Sang-Hee</creatorcontrib><creatorcontrib>Jung, Hong Dae</creatorcontrib><creatorcontrib>Kwon, Kyung-Sool</creatorcontrib><creatorcontrib>Kim, Moon-Bum</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>International journal of dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Byung Soo</au><au>Seo, Sang-Hee</au><au>Jung, Hong Dae</au><au>Kwon, Kyung-Sool</au><au>Kim, Moon-Bum</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>X-Linked reticulate pigmentary disorder in a female patient</atitle><jtitle>International journal of dermatology</jtitle><addtitle>Int J Dermatol</addtitle><date>2010-04</date><risdate>2010</risdate><volume>49</volume><issue>4</issue><spage>421</spage><epage>425</epage><pages>421-425</pages><issn>0011-9059</issn><eissn>1365-4632</eissn><coden>IJDEBB</coden><abstract>Background X‐Linked reticulate pigmentary disorder is a very rare cutaneous condition characterized by different clinical manifestations according to sex.
Methods We report a 31‐year‐old woman with X‐linked reticulate pigmentary disorder.
Results On examination, there were multiple, asymptomatic, brownish macules in linear and whorled patterns over the trunk, axillae, groin, and extremities. The woman had not experienced any systemic manifestations involving the gastrointestinal, pulmonary, or ocular systems. Her hair, teeth, and nails were normal on close observation. All laboratory data were within the normal range. A genetic study was not performed.
Conclusions Although a genetic study was not performed, we believe that our patient can be diagnosed with X‐linked reticulate pigmentary disorder according to the clinical and histopathologic findings.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>20465698</pmid><doi>10.1111/j.1365-4632.2010.04102.x</doi><tpages>5</tpages></addata></record> |
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| subjects | Adult Biological and medical sciences Dermatology Female Genetic Diseases, X-Linked - diagnosis Genetic Diseases, X-Linked - pathology Humans Hyperpigmentation - diagnosis Hyperpigmentation - genetics Medical sciences Pigmentary diseases of the skin |
| title | X-Linked reticulate pigmentary disorder in a female patient |
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