{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,21]],"date-time":"2024-05-21T04:28:14Z","timestamp":1716265694385},"reference-count":8,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,9,17]]},"DOI":"10.7759\/cureus.18061","type":"journal-article","created":{"date-parts":[[2021,9,17]],"date-time":"2021-09-17T19:17:00Z","timestamp":1631906220000},"source":"Crossref","is-referenced-by-count":1,"title":["A Case of Mal De Meleda: The Rare Presentation of Palmoplantar Keratoderma Disease"],"prefix":"10.7759","author":[{"given":"Vamsi","family":"Kalyan","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tarun K","family":"Suvvari","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Venkata Dinesh Kumar","family":"Kandula","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aparajeya","family":"Shanker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lolita","family":"Matiashova","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1007\/s40257-015-0157-1","article-title":"Mal de Meleda: a focused review","volume":"17","author":"Perez C","year":"2016","unstructured":"Perez C, Khachemoune A. Mal de Meleda: a focused review. Am J Clin Dermatol. 2016, 17:63-70. 10.1007\/s40257-015-0157-1","journal-title":"Am J Clin Dermatol"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1155\/2013\/206803","article-title":"Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region","volume":"2013","author":"Bchetnia M","year":"2013","unstructured":"Bchetnia M, Laroussi N, Youssef M, et al.. Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region. Biomed Res Int. 2013, 2013:206803. 10.1155\/2013\/206803","journal-title":"Biomed Res Int"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.4103\/0019-5154.100497","article-title":"Mal de Meleda with lip involvement: a report of two cases","volume":"57","author":"Nath AK","year":"2012","unstructured":"Nath AK, Chaudhuri S, Thappa DM. Mal de Meleda with lip involvement: a report of two cases. Indian J Dermatol. 2012, 57:390-393. 10.4103\/0019-5154.100497","journal-title":"Indian J Dermatol"},{"key":"ref4","article-title":"Greither's disease","volume":"69","author":"Athanikar SB","year":"2003","unstructured":"Athanikar SB, Inamadar AC, Palit A, Sampagavi VV, Deshmukh NS. Greither's disease. Indian J Dermatol Venereol Leprol. 2003, 69:292-293.","journal-title":"Indian J Dermatol Venereol Leprol"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1046\/j.1525-1470.2003.20319.x","article-title":"What syndrome is this? Greither syndrome","volume":"20","author":"Tay YK","year":"2003","unstructured":"Tay YK. What syndrome is this? Greither syndrome. Pediatr Dermatol. 2003, 20:272-275. 10.1046\/j.1525-1470.2003.20319.x","journal-title":"Pediatr Dermatol"},{"key":"ref6","article-title":"Disorders of Keratinization","author":"Judge MR","year":"2010","unstructured":"Judge MR, McLean WH, Munro CS. Disorders of Keratinization. Rook's Textbook of Dermatology. Burns T, Breathnach S, Cox N, Griffiths C (ed): Oxford: Blackwell Science, Singapore; 2010. 8:19.93-19.119."},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.4103\/0378-6323.42930","article-title":"Huriez syndrome","volume":"74","author":"Sekar SC","year":"2008","unstructured":"Sekar SC, Srinivas CR. Huriez syndrome. Indian J Dermatol Venereol Leprol. 2008, 74:409-410. 10.4103\/0378-6323.42930","journal-title":"Indian J Dermatol Venereol Leprol"},{"key":"ref8","article-title":"Keratoderma hereditaria mutilans (vohwinkel's syndrome)","volume":"63","author":"Dayal S","year":"1997","unstructured":"Dayal S, Jain VK, Singh H. Keratoderma hereditaria mutilans (vohwinkel's syndrome). Indian J Dermatol Venereol Leprol. 1997, 63:186-188.","journal-title":"Indian J Dermatol Venereol Leprol"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/71386-a-case-of-mal-de-meleda-the-rare-presentation-of-palmoplantar-keratoderma-disease","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,9]],"date-time":"2024-02-09T19:29:59Z","timestamp":1707506999000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/71386-a-case-of-mal-de-meleda-the-rare-presentation-of-palmoplantar-keratoderma-disease"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,9,17]]},"references-count":8,"URL":"https:\/\/doi.org\/10.7759\/cureus.18061","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2021,9,17]]}}}