{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T18:26:40Z","timestamp":1777660000651,"version":"3.51.4"},"reference-count":0,"publisher":"SAGE Publications","issue":"4","license":[{"start":{"date-parts":[[2008,12,1]],"date-time":"2008-12-01T00:00:00Z","timestamp":1228089600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Genetic Testing"],"published-print":{"date-parts":[[2008,12,1]]},"abstract":"<jats:p>\n                    Sclerosteosis is a severe, rare, autosomal recessive bone condition that is characterized by a progressive craniotubular hyperostosis. The main features are a significant sclerosis of the long bones, ribs, pelvis, and skull, leading to facial distortion and entrapment of cranial nerves. Clinical features include a tall stature, nail dysplasia, cutaneous syndactyly of some fingers, and raised intracranial pressure. The sclerosteosis gene has been mapped to chromosome 17q12\u201321 and is currently known as the\n                    <jats:italic toggle=\"yes\">SOST<\/jats:italic>\n                    gene encoding the sclerostin protein. Here, we report on one familial and one isolated case of Brazilian origin with the clinical and molecular diagnosis of sclerosteosis. The radiological and clinical features are described, and the diagnosis of sclerosteosis was confirmed in both cases by mutation analysis of the\n                    <jats:italic toggle=\"yes\">SOST<\/jats:italic>\n                    gene showing a homozygous nonsense mutation (Trp124X) in the two patients. We reported this mutation previously in other sclerosteosis patients from a consanguineous Brazilian family. Interestingly, all three families were from the same state in Brazil, but they denied familial relationship. These patients confirm the clinical picture as found in other cases with a loss of function mutation in the\n                    <jats:italic toggle=\"yes\">SOST<\/jats:italic>\n                    gene.\n                  <\/jats:p>","DOI":"10.1089\/gte.2008.0036","type":"journal-article","created":{"date-parts":[[2008,12,15]],"date-time":"2008-12-15T09:06:08Z","timestamp":1229331968000},"page":"475-479","source":"Crossref","is-referenced-by-count":30,"title":["A Known\n                    <i>SOST<\/i>\n                    Gene Mutation Causes Sclerosteosis in a Familial and an Isolated Case from Brazilian Origin"],"prefix":"10.1177","volume":"12","author":[{"given":"Chong Ae","family":"Kim","sequence":"first","affiliation":[{"name":"Hospital das Cl\u00ednicas","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rachel","family":"Honjo","sequence":"additional","affiliation":[{"name":"Hospital das Cl\u00ednicas","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D\u00e9bora","family":"Bertola","sequence":"additional","affiliation":[{"name":"Hospital das Cl\u00ednicas","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"L\u00edlian","family":"Albano","sequence":"additional","affiliation":[{"name":"Hospital das Cl\u00ednicas","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Luiz","family":"Oliveira","sequence":"additional","affiliation":[{"name":"Hospital das Cl\u00ednicas","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sumatra","family":"Jales","sequence":"additional","affiliation":[{"name":"HC\/FMUSP","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jos\u00e9","family":"Siqueira","sequence":"additional","affiliation":[{"name":"HC\/FMUSP","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Arthur","family":"Castilho","sequence":"additional","affiliation":[{"name":"HC\/FMUSP","place":["Brazil"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wendy","family":"Balemans","sequence":"additional","affiliation":[{"name":"University of Antwerp","place":["Belgium"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elke","family":"Piters","sequence":"additional","affiliation":[{"name":"University of Antwerp","place":["Belgium"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Karen","family":"Jennes","sequence":"additional","affiliation":[{"name":"University of Antwerp","place":["Belgium"]}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wim","family":"Van Hul","sequence":"additional","affiliation":[{"name":"University of Antwerp","place":["Belgium"]}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2008,12,15]]},"container-title":["Genetic Testing"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1089\/gte.2008.0036","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.sagepub.com\/doi\/pdf\/10.1089\/gte.2008.0036","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,4,29]],"date-time":"2026-04-29T07:21:15Z","timestamp":1777447275000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.sagepub.com\/doi\/10.1089\/gte.2008.0036"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2008,12,1]]},"references-count":0,"journal-issue":{"issue":"4","published-print":{"date-parts":[[2008,12,1]]}},"alternative-id":["10.1089\/gte.2008.0036"],"URL":"https:\/\/doi.org\/10.1089\/gte.2008.0036","relation":{},"ISSN":["1090-6576","1557-7473"],"issn-type":[{"value":"1090-6576","type":"print"},{"value":"1557-7473","type":"electronic"}],"subject":[],"published":{"date-parts":[[2008,12,1]]}}}