{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,18]],"date-time":"2026-10-18T01:03:45Z","timestamp":1792285425767,"version":"4.4.0"},"reference-count":41,"publisher":"Wiley","issue":"1","license":[{"start":{"date-parts":[[2011,6,30]],"date-time":"2011-06-30T00:00:00Z","timestamp":1309392000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Clinical Genetics"],"published-print":{"date-parts":[[2012,7]]},"abstract":"<jats:p>Roudgari H, Farndon PA, Murray AD, Hardy C, Miedzybrodzka Z. Is <jats:italic>PATCHED<\/jats:italic> an important candidate gene for neural tube defects? Cranial and thoracic neural tube defects in a family with Gorlin syndrome: a case report.<\/jats:p><jats:p>The relationship of mutations in the patched gene <jats:italic>PTCH<\/jats:italic> and nevoid basal cell carcinoma (NBCC) or Gorlin syndrome is well established. Animal studies have implicated the hedgehog\u2010patched signalling pathway in neurulation and neural tube defects (NTDs). Spina bifida occulta and bifid vertebrae are well recognized in NBCCS, but there appears to be only one report of open spina bifida. We report a father and two sons with a truncating <jats:italic>PTCH<\/jats:italic> mutation and the major features of NBCCS. One son had open thoracic spina bifida and the other had an occipital meningocoele. We believe this to be the first report of cranial NTD in NBCCS and suggest that consideration be given to including PTCH analysis in genetic association studies in NTDs as the hedgehog pathway is integral to normal human neurulation.<\/jats:p>","DOI":"10.1111\/j.1399-0004.2011.01725.x","type":"journal-article","created":{"date-parts":[[2011,6,8]],"date-time":"2011-06-08T19:37:37Z","timestamp":1307561857000},"page":"71-76","source":"Crossref","is-referenced-by-count":10,"title":["Is <i>PATCHED<\/i> an important candidate gene for neural tube defects? 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