{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T10:37:36Z","timestamp":1788863856980,"version":"build-2803163510"},"reference-count":21,"publisher":"Oxford University Press (OUP)","issue":"3","license":[{"start":{"date-parts":[[2015,9,1]],"date-time":"2015-09-01T00:00:00Z","timestamp":1441065600000},"content-version":"tdm","delay-in-days":2344,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2009,4]]},"DOI":"10.1111\/j.1365-2230.2008.03074.x","type":"journal-article","created":{"date-parts":[[2009,1,13]],"date-time":"2009-01-13T16:05:22Z","timestamp":1231862722000},"page":"319-323","source":"Crossref","is-referenced-by-count":92,"title":["Cutis marmorata telangiectatica congenita: a prospective study of 27 cases and review of the literature with proposal of diagnostic criteria"],"prefix":"10.1093","volume":"34","author":[{"given":"A. K.","family":"Kienast","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P. H.","family":"Hoeger","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"286","reference":[{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB1","first-page":"202","article-title":"\u00dcber eine seltene angeborene Hautanomalie [Cutis marmorata telangiectatica congenita]","volume":"3","author":"Van Lohuizen","year":"1922","journal-title":"Acta Derm Venereol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB2","doi-asserted-by":"crossref","first-page":"950","DOI":"10.1067\/mjd.2003.301","article-title":"Cutis marmorata telangiectatica congenita with hemangiomatous histopathologic features","volume":"48","author":"Fujita","year":"2003","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB3","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1111\/j.1600-0560.1974.tb00188.x","article-title":"Cutis marmorata telangiectatica congenita","volume":"1","author":"Way","year":"1974","journal-title":"J Cutan Pathol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB4","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1046\/j.1525-1470.2000.01723.x","article-title":"Cutis marmorata telangiectatica congenita: clinical findings in 85 patients","volume":"17","author":"Amitai","year":"2000","journal-title":"Pediatr Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB5","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1001\/archderm.135.1.34","article-title":"Cutis marmorata telangiectatica congenita. Clinical features in 35 cases","volume":"135","author":"Devillers","year":"1999","journal-title":"Arch Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB6","first-page":"117","article-title":"MRI and neurological findings in macrocephaly-cutis marmorata telangiectatica congenita syndrome: report of ten cases and review of the literature","volume":"16","author":"Garavelli","year":"2005","journal-title":"Genet Couns"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB7","doi-asserted-by":"crossref","first-page":"99","DOI":"10.1002\/ajmg.a.20551","article-title":"Macrocephaly-cutis marmorata telangiectatica congenita: seven cases including two with unusual cerebral manifestations","volume":"126A","author":"Giuliano","year":"2004","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB8","doi-asserted-by":"crossref","first-page":"6","DOI":"10.1111\/j.1525-1470.1993.tb00002.x","article-title":"Cutis marmorata telangiectatica congenita: long-term follow-up, review of the literature and report of a case in conjunction with congenital hypothyroidism","volume":"10","author":"Pehr","year":"1993","journal-title":"Pediatr Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB9","doi-asserted-by":"crossref","first-page":"1098","DOI":"10.1016\/S0190-9622(89)70140-7","article-title":"Cutis marmorata telangiectatica congenita. Report of 22 cases","volume":"20","author":"Picascia","year":"1989","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB10","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1016\/S0190-9622(96)90354-0","article-title":"Association of glaucoma with cutis marmorata telangiectatica congenita: a localized anatomic malformation","volume":"35","author":"Weilepp","year":"1996","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB11","doi-asserted-by":"crossref","first-page":"294","DOI":"10.1002\/ajmg.a.30221","article-title":"Abnormal pericyte recruitment as a cause for pulmonary hypertension in Adams-Oliver syndrome","volume":"129","author":"Patel","year":"2004","journal-title":"Am J Med Genet"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB12","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1097\/00019605-199710000-00001","article-title":"Macrocephaly with cutis marmorata, haemangioma and syndactyly - a distinctive overgrowth syndrome","volume":"6","author":"Clayton-Smith","year":"1997","journal-title":"Clin Dysmorphol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB13","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1002\/(SICI)1096-8628(19970502)70:1<67::AID-AJMG13>3.0.CO;2-V","article-title":"Macrocephaly-cutis marmorata telangiectatica congenita: a distinctive disorder with developmental delay and connective tissue abnormalities","volume":"70","author":"Moore","year":"1997","journal-title":"Am J Med Genet"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB14","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1002\/ajmg.a.30235","article-title":"Macrocephaly-cutis marmorata telangiectatica congenita. Report of six new patients and a review","volume":"130A","author":"Lapunzina","year":"2004","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB15","article-title":"Accurately renaming macrocephaly-cutis marmorata telangiectatica congenita (M-CMTC) as macrocephaly-capillary malformation (M-CM)","volume":"143","author":"Torriello","year":"2007","journal-title":"Am J Med Genet A"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB16","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1002\/(SICI)1096-8628(20000214)90:4<265::AID-AJMG1>3.0.CO;2-S","article-title":"Macrocephaly-cutis marmorata telangiectatica congenita without cutis marmorata?","volume":"90","author":"Franceschini","year":"2000","journal-title":"Am J Med Genet"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB17","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1016\/j.jaad.2007.11.018","article-title":"Macrocephaly-cutis marmorata telangiectatica congenita: a case report and review of salient features","volume":"58","author":"Katugampola","year":"2008","journal-title":"J Am Acad Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB18","doi-asserted-by":"crossref","first-page":"356","DOI":"10.1111\/j.1525-1470.2007.00496.x","article-title":"Reticular infantile hemangioma of the limb can be associated with ventral-caudal anomalies, refractory ulceration, and cardiac overload","volume":"24","author":"Mulliken","year":"2007","journal-title":"Pediatr Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB19","doi-asserted-by":"crossref","first-page":"366","DOI":"10.1046\/j.1365-2133.2000.03311.x","article-title":"Cutis marmorata telangiectatica congenita: report of 18 cases","volume":"142","author":"Gerritsen","year":"2000","journal-title":"Br J Dermatol"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB20","doi-asserted-by":"crossref","first-page":"944","DOI":"10.1016\/S0022-3476(78)81216-5","article-title":"Cutis marmorata telangiectatica congenita (congenital generalized phlebectasia)","volume":"93","author":"South","year":"1978","journal-title":"J Pediatr"},{"key":"10.1111\/j.1365-2230.2008.03074.x-BIB21","doi-asserted-by":"crossref","first-page":"21","DOI":"10.1007\/s001050050541","article-title":"Cutis marmorata telangiectatica congenita","volume":"48","author":"Rupprecht","year":"1997","journal-title":"Der Hautarzt"}],"container-title":["Clinical and Experimental Dermatology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.wiley.com\/onlinelibrary\/tdm\/v1\/articles\/10.1111%2Fj.1365-2230.2008.03074.x","content-type":"unspecified","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/onlinelibrary.wiley.com\/wol1\/doi\/10.1111\/j.1365-2230.2008.03074.x\/fullpdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,2,14]],"date-time":"2023-02-14T14:27:42Z","timestamp":1676384862000},"score":1,"resource":{"primary":{"URL":"https:\/\/academic.oup.com\/ced\/article\/34\/3\/319\/6624703"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,4]]},"references-count":21,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2009,4]]}},"URL":"https:\/\/doi.org\/10.1111\/j.1365-2230.2008.03074.x","relation":{},"ISSN":["0307-6938","1365-2230"],"issn-type":[{"value":"0307-6938","type":"print"},{"value":"1365-2230","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,4]]}}}