{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,4,16]],"date-time":"2026-04-16T01:48:00Z","timestamp":1776304080704,"version":"3.50.1"},"reference-count":23,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2008,7]]},"DOI":"10.1097\/mcd.0b013e3282f4a10e","type":"journal-article","created":{"date-parts":[[2008,6,2]],"date-time":"2008-06-02T07:06:17Z","timestamp":1212390377000},"page":"165-168","source":"Crossref","is-referenced-by-count":2,"title":["Localized acalvaria with craniosynostosis"],"prefix":"10.1097","volume":"17","author":[{"given":"Eissa","family":"Faqeih","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zoltan","family":"Patay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zuhair","family":"Rahbeeni","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jamila","family":"Murtada","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Essam","family":"Al Shail","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Judith G.","family":"Hall","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-3-20211004","doi-asserted-by":"crossref","first-page":"353","DOI":"10.1097\/00019605-199410000-00013","article-title":"Fetus with features of Crane-Heise syndrome and aminopterin syndrome sine aminopterin","volume":"3","author":"Barnicoat","year":"1994","journal-title":"Clin Dysmorphol"},{"key":"R2-3-20211004","doi-asserted-by":"crossref","first-page":"399","DOI":"10.1002\/tera.1420500606","article-title":"Teratogen update: angiotensin-converting enzyme inhibitors","volume":"50","author":"Barr","year":"1994","journal-title":"Teratology"},{"key":"R3-3-20211004","doi-asserted-by":"crossref","first-page":"485","DOI":"10.1002\/tera.1420440503","article-title":"ACE inhibitor fetopathy and hypocalvaria: the kidney-skull connection","volume":"44","author":"Barr","year":"1991","journal-title":"Teratology"},{"key":"R4-3-20211004","doi-asserted-by":"crossref","first-page":"F11","DOI":"10.1136\/fn.82.1.F11","article-title":"Fetal acalvaria with amniotic band syndrome","volume":"82","author":"Chandran","year":"2000","journal-title":"Arch Dis Child Fetal Neonatal Ed"},{"key":"R5-3-20211004","doi-asserted-by":"crossref","first-page":"235","DOI":"10.1542\/peds.68.2.235","article-title":"New syndrome in three affected siblings","volume":"68","author":"Crane","year":"1981","journal-title":"Pediatrics"},{"key":"R6-3-20211004","doi-asserted-by":"crossref","first-page":"363","DOI":"10.1002\/jcu.1870190608","article-title":"Sonographic diagnosis of fetal acrania","volume":"19","author":"Ekici","year":"1991","journal-title":"J Clin Ultrasound"},{"key":"R7-3-20211004","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1002\/ajmg.1320490331","article-title":"Acalvaria and occipital scalp defects","volume":"49","author":"Fryns","year":"1994","journal-title":"Am J Med Genet"},{"key":"R8-3-20211004","doi-asserted-by":"crossref","first-page":"694","DOI":"10.1002\/ajmg.1320460620","article-title":"Acalvaria: a unique congenital anomaly","volume":"46","author":"Harris","year":"1993","journal-title":"Am J Med Genet"},{"key":"R9-3-20211004","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1097\/00001665-200403000-00002","article-title":"A case study of amnion rupture sequence with acalvaria, blindness, and clefting: clinical and psychological profiles","volume":"15","author":"Hukki","year":"2004","journal-title":"J Craniofac Surg"},{"key":"R10-3-20211004","doi-asserted-by":"crossref","first-page":"433","DOI":"10.1007\/s100249900059","article-title":"Neonatal hemochromatosis, renal tubular dysgenesis and hypocalvaria in a neonate","volume":"1","author":"Johal","year":"1998","journal-title":"Pediatr Dev Pathol"},{"key":"R11-3-20211004","doi-asserted-by":"crossref","first-page":"783","DOI":"10.7863\/jum.1999.18.11.783","article-title":"Acalvaria and hydrocephalus: a case report and discussion of the literature","volume":"18","author":"Kathleen","year":"1999","journal-title":"J Ultrasound Med"},{"key":"R12-3-20211004","first-page":"618","article-title":"Acalvaria","volume":"41","author":"Khadilkar","year":"2004","journal-title":"Indian Pediatr"},{"key":"R13-3-20211004","doi-asserted-by":"crossref","first-page":"52","DOI":"10.1159\/000121015","article-title":"Acrania: report of the first surviving case","volume":"24","author":"Kurata","year":"1996","journal-title":"Pediatr Neurosurg"},{"key":"R14-3-20211004","first-page":"1","article-title":"Acrania: review of 13 cases","volume":"1","author":"Kwon","year":"1991","journal-title":"The Fetus"},{"key":"R15-3-20211004","doi-asserted-by":"crossref","first-page":"265","DOI":"10.1002\/ajmg.1320360302","article-title":"An unusual type of acrocephalosyndactyly with bilateral parietooccipital \u2018encephalocele,\u2019 micropenis, and severe mental retardation","volume":"36","author":"Lorenz","year":"1990","journal-title":"Am J Med Genet"},{"key":"R16-3-20211004","doi-asserted-by":"crossref","first-page":"181","DOI":"10.2214\/ajr.139.1.181","article-title":"Sonographic demonstration of fetal acrania","volume":"139","author":"Mannes","year":"1982","journal-title":"AJR"},{"key":"R17-3-20211004","doi-asserted-by":"crossref","first-page":"593","DOI":"10.1067\/mpd.2002.127650","article-title":"Primary acalvaria in a term newborn","volume":"141","author":"Raupp","year":"2002","journal-title":"J Pediatr"},{"key":"R18-3-20211004","doi-asserted-by":"crossref","first-page":"293","DOI":"10.1055\/s-2003-42692","article-title":"Antenatal imaging of a near-term fetus with primary acalvaria","volume":"20","author":"Raupp","year":"2003","journal-title":"Am J Perinatol"},{"key":"R19-3-20211004","doi-asserted-by":"crossref","first-page":"452","DOI":"10.1007\/s003830000511","article-title":"Agenesis of the skull bones","volume":"17","author":"Sharma","year":"2001","journal-title":"Pediatr Surg Int"},{"issue":"Suppl","key":"R20-3-20211004","first-page":"319","article-title":"Acalvaria, holoprosencephaly, and facial dysmorphism syndrome","volume":"2","author":"Sperber","year":"1986","journal-title":"J Craniofac Genet Dev Biol"},{"key":"R21-3-20211004","doi-asserted-by":"crossref","first-page":"715","DOI":"10.7863\/jum.1987.6.12.715","article-title":"Antenatal diagnosis of fetal acrania","volume":"6","author":"Vergani","year":"1987","journal-title":"J Ultrasound Med"},{"key":"R22-3-20211004","doi-asserted-by":"crossref","first-page":"413","DOI":"10.1136\/jmg.22.5.413-a","article-title":"Parietal foramina in the Saethre-Chotzen syndrome","volume":"22","author":"Young","year":"1985","journal-title":"J Med Genet"},{"key":"R23-3-20211004","doi-asserted-by":"crossref","first-page":"223","DOI":"10.1002\/ajmg.a.10026","article-title":"Crane-Heise syndrome: a second familial case report with elaboration of phenotype","volume":"118","author":"Zand","year":"2003","journal-title":"Am J Med Genet"}],"container-title":["Clinical Dysmorphology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/00019605-200807000-00003","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,2,26]],"date-time":"2024-02-26T23:20:22Z","timestamp":1708989622000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00019605-200807000-00003"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,7]]},"references-count":23,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2008]]}},"URL":"https:\/\/doi.org\/10.1097\/mcd.0b013e3282f4a10e","relation":{},"ISSN":["0962-8827"],"issn-type":[{"value":"0962-8827","type":"print"}],"subject":[],"published":{"date-parts":[[2008,7]]}}}