{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T14:20:08Z","timestamp":1787840408948,"version":"build-2784847793"},"reference-count":9,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2012,7]]},"abstract":"<jats:p>Congenital alopecia includes a broad differential diagnosis and presents a diagnostic and therapeutic challenge for the physician. Congenital atrichia is a rare form of irreversible alopecia that is usually inherited as an autosomal recessive pattern. We report a 2-year-old male child presenting with total alopecia of scalp, eyebrows, eyelashes, and body hair since birth. The child had cardiac malposition with situs inversus of the viscera. Computed tomography of the chest and abdomen revealed median position of the heart with transposition of abdominal viscera. To our knowledge, this is the first case of congenital atrichia associated with situs inversus and mesocardia.<\/jats:p>","DOI":"10.4103\/0974-7753.100093","type":"journal-article","created":{"date-parts":[[2014,1,30]],"date-time":"2014-01-30T02:25:20Z","timestamp":1391048720000},"page":"181-183","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":5,"title":["Congenital Atrichia Associated with Situs Inversus and Mesocardia"],"prefix":"10.4103","volume":"4","author":[{"given":"S","family":"Sacchidanand","sequence":"first","affiliation":[{"name":"Department of Dermatology, STD and Leprosy, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"MS","family":"Sahana","sequence":"additional","affiliation":[{"name":"Department of Dermatology, STD and Leprosy, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ravi","family":"Hiremagalore","sequence":"additional","affiliation":[{"name":"Department of Dermatology, STD and Leprosy, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"GS","family":"Asha","sequence":"additional","affiliation":[{"name":"Department of Dermatology, STD and Leprosy, Bangalore Medical College and Research Institute, Bangalore, Karnataka, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R2-20250606","doi-asserted-by":"crossref","first-page":"72","DOI":"10.1159\/000247092","article-title":"Isolated congenital atrichia in an Omani Kindred","volume":"188","author":"Kenue","year":"1994","journal-title":"Dermatology"},{"key":"R3-20250606","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1111\/j.1440-0960.1964.tb01355.x","article-title":"Congenital atrichia","volume":"7","author":"Linn","year":"1964","journal-title":"Aust J Dermatol"},{"key":"R4-20250606","doi-asserted-by":"crossref","first-page":"887","DOI":"10.1046\/j.1523-1747.2001.01767.x","article-title":"Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions","volume":"118","author":"Zlotogorski","year":"2002","journal-title":"J Invest Dermatol"},{"key":"R5-20250606","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1136\/jmg.20.1.64","article-title":"A new alopecia\/mental retardation syndrome","volume":"20","author":"Baraitser","year":"1983","journal-title":"J Med Genet"},{"key":"R6-20250606","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1046\/j.0022-202x.2001.01689.x","article-title":"A novel connexin 30 mutation in Clouston syndrome","volume":"118","author":"Smith","year":"2002","journal-title":"J Invest Dermatol"},{"key":"R7-20250606","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1046\/j.1365-4362.1999.00005.x","article-title":"Congenital hypotrichosis","volume":"38","author":"De Berker","year":"1998","journal-title":"Int J Dermatol"},{"key":"R8-20250606","doi-asserted-by":"crossref","first-page":"386","DOI":"10.1086\/301717","article-title":"A gene for congenital alopecia maps to chromosome 8p21-8p22","volume":"62","author":"N\u00f6then","year":"1998","journal-title":"Am J Hum Genet"},{"key":"R9-20250606","doi-asserted-by":"crossref","first-page":"343","DOI":"10.1001\/archderm.141.3.343","article-title":"The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: A comparative clinical, histologic, and immunohistochemical study","volume":"141","author":"Bergman","year":"2005","journal-title":"Arch Dermatol"},{"key":"R10-20250606","doi-asserted-by":"crossref","first-page":"1352","DOI":"10.1016\/j.amjcard.2011.06.055","article-title":"The cardiac malpositions","volume":"108","author":"Perloff","year":"2011","journal-title":"Am J Cardiol"}],"container-title":["International Journal of Trichology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/01437809-201204030-00012","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,27]],"date-time":"2026-08-27T13:22:12Z","timestamp":1787836932000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/01437809-201204030-00012"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,7]]},"references-count":9,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2012]]}},"URL":"https:\/\/doi.org\/10.4103\/0974-7753.100093","relation":{},"ISSN":["0974-7753","0974-9241"],"issn-type":[{"value":"0974-7753","type":"print"},{"value":"0974-9241","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,7]]}}}