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Cystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature

DC FieldValueLanguage
dc.contributor.author지헌영-
dc.date.accessioned2018-07-20T08:16:34Z-
dc.date.available2018-07-20T08:16:34Z-
dc.date.issued2017-
dc.identifier.issn1552-4825-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/161034-
dc.description.abstractWalker-Warburg syndrome (WWS) is a severe form of congenital muscular dystrophy secondary to α-dystroglycanopathy with muscle, brain, and eye abnormalities often leading to death in the first weeks of life. It is transmitted in an autosomal recessive pattern, and has been linked to at least 15 different genes; including protein O-mannosyltransferase 1 (POMT1), protein O-mannosyltransferase 2 (POMT2), protein O-mannose beta-1,2-N acetylglucosaminyltransferase (POMGNT1), fukutin (FKTN), isoprenoid synthase domain-containing protein (ISPD), and other genes. We report on a consanguineous family with four consecutive siblings affected by this condition with lethal outcome in three (still birth), and termination of the fourth pregnancy based on antenatal MRI identification of brain and kidney anomalies that heralded proper and deep clinical phenotyping. The diagnosis of WWS was suggested based on the unique collective phenotype comprising brain anomalies in the form of lissencephaly, subcortical/subependymal heterotopia, and cerebellar hypoplasia shared by all four siblings; microphthalmia in one sibling; and large cystic kidneys in the fetus and another sibling. Other unshared neurological abnormalities included hydrocephalus and Dandy-Walker malformation. Whole exome sequencing of the fetus revealed a highly conserved missense mutation in POMT2 that is known to cause WWS with brain and eye anomalies.In conclusion, the heterogeneous clinical presentation in the four affected conceptions with POMT2 mutation expands the current clinical spectrum of POMT2-associated WWS to include large cystic kidneys; and confirms intra-familial variability in terms of brain, kidney, and eye anomalies.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.relation.isPartOfAMERICAN JOURNAL OF MEDICAL GENETICS PART A-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHFemale-
dc.subject.MESHFetal Diseases/genetics-
dc.subject.MESHFetal Diseases/pathology*-
dc.subject.MESHGenetic Predisposition to Disease-
dc.subject.MESHHumans-
dc.subject.MESHKidney Diseases, Cystic/etiology-
dc.subject.MESHKidney Diseases, Cystic/pathology*-
dc.subject.MESHMale-
dc.subject.MESHMannosyltransferases/genetics*-
dc.subject.MESHMutation, Missense*-
dc.subject.MESHPedigree-
dc.subject.MESHPhenotype-
dc.subject.MESHPregnancy-
dc.subject.MESHSiblings-
dc.subject.MESHWalker-Warburg Syndrome/complications*-
dc.subject.MESHWalker-Warburg Syndrome/genetics-
dc.subject.MESHWhole Exome Sequencing/methods-
dc.titleCystic kidneys in fetal Walker-Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Pharmacology-
dc.contributor.googleauthorMarwa M. Nabhan-
dc.contributor.googleauthorNour ElKhateeb-
dc.contributor.googleauthorDaniela A. Braun-
dc.contributor.googleauthorSungho Eun-
dc.contributor.googleauthorSahar N. Saleem-
dc.contributor.googleauthorHeon YungGee-
dc.contributor.googleauthorFriedhelm Hildebrandt-
dc.contributor.googleauthorNeveen A. Soliman-
dc.identifier.doi10.1002/ajmg.a.38393-
dc.contributor.localIdA03971-
dc.relation.journalcodeJ00091-
dc.identifier.eissn1552-4833-
dc.identifier.pmid28815891-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.a.38393-
dc.subject.keywordWalker-Warburg syndrome-
dc.subject.keywordcystic kidneys-
dc.subject.keywordwhole exome sequencing-
dc.contributor.alternativeNameGee, Heon Yung-
dc.contributor.affiliatedAuthorGee, Heon Yung-
dc.citation.volume173-
dc.citation.number10-
dc.citation.startPage2697-
dc.citation.endPage2702-
dc.identifier.bibliographicCitationAMERICAN JOURNAL OF MEDICAL GENETICS PART A, Vol.173(10) : 2697-2702, 2017-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers

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