{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,18]],"date-time":"2026-10-18T00:55:46Z","timestamp":1792284946445,"version":"4.4.0"},"reference-count":3,"publisher":"BMJ","issue":"7","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Med Genet"],"published-print":{"date-parts":[[1998,7]]},"abstract":"<jats:p>Aplasia cutis congenita is a heterogeneous group of conditions usually involving the scalp as well as any other part of the body and is associated with a number of other congenital anomalies. We report on a newborn male with almost complete absence of skin and subcutaneous tissue in association with choanal atresia, syndactyly, imperforate anus, pulmonary hypoplasia, and other anomalies. To our knowledge, this condition, not only in the extent of the lesion but the associated anomalies, has not been reported previously.<\/jats:p>","DOI":"10.1136\/jmg.35.7.609","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T15:37:21Z","timestamp":1226331441000},"page":"609-611","source":"Crossref","is-referenced-by-count":11,"title":["Extensive form of aplasia cutis congenita: a new syndrome?"],"prefix":"10.1136","volume":"35","author":[{"given":"M S","family":"Park","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S H","family":"Hahn","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C H","family":"Hong","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J S","family":"Kim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H S","family":"Kim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","published-online":{"date-parts":[[1998,7,1]]},"reference":[{"key":"ref_1","article-title":"Aplasia cutis congenita: a clinical review and p6r4o6p-o6s0a.l for classification","author":"Frieden, I.J.","year":"1986","unstructured":"Frieden IJ. Aplasia cutis congenita: a clinical review and p6r4o6p-o6s0a.l for classification. J Am Acad Dermatol 1986;14: Sly1i4be.seratnVdP.reAvpileawsioaf cutis congenita: a report of 12 the literature. Pediatr Dematol new fami-","journal-title":"J Am Acad Dermatol; 14: Sly1i4be.seratnVdP.reAvpileawsioaf cutis congenita: a report of 12 the literature"},{"key":"ref_2","article-title":"Extensive symmetric truncal aplasia cutis congenita without fetus papyraceus or macroscopic evidence of placental abnormalities. Pediatr Dematol 1995; 12: non dermis or epidermio s. There was no hyperkeratosis which is a consistent findi","author":"Boente, M.C.; Frontini, M.V.; Acosta, M.I.; Saleme, C.; Barrionuevo, S.; Asial, R.","unstructured":"Boente MC, Frontini MV, Acosta MI, Saleme C, Barrionuevo S, Asial R. Extensive symmetric truncal aplasia cutis congenita without fetus papyraceus or macroscopic evidence of placental abnormalities. Pediatr Dematol 1995;12: non dermis or epidermio s. There was no hyperkeratosis which is a consistent findi. ng"},{"key":"ref_3","first-page":"45","article-title":"Johanson-Blizzard syndrome. _7 Med","volume":"26","author":"Hurst, J.A.; Baraitser, M.","year":"1989","unstructured":"Hurst JA, Baraitser M. Johanson-Blizzard syndrome. _7 Med Genet 1989;26:45-8.","journal-title":"Genet"}],"container-title":["Journal of Medical Genetics"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jmg.35.7.609","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,5]],"date-time":"2025-10-05T18:03:51Z","timestamp":1759687431000},"score":1,"resource":{"primary":{"URL":"https:\/\/jmg.bmj.com\/lookup\/doi\/10.1136\/jmg.35.7.609"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1998,7]]},"references-count":3,"journal-issue":{"issue":"7","published-online":{"date-parts":[[1998,7,1]]},"published-print":{"date-parts":[[1998,7]]}},"alternative-id":["10.1136\/jmg.35.7.609"],"URL":"https:\/\/doi.org\/10.1136\/jmg.35.7.609","relation":{},"ISSN":["0022-2593","1468-6244"],"issn-type":[{"value":"0022-2593","type":"print"},{"value":"1468-6244","type":"electronic"}],"subject":[],"published":{"date-parts":[[1998,7]]}}}