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Polydactyly and fetal hydantoin syndrome: An additional component of the syndrome?

dc.contributor.authorCENANI, A
dc.contributor.authorYALCINKAYA, Cengiz
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorSOMAY, G
dc.date.accessioned2021-03-03T17:17:06Z
dc.date.available2021-03-03T17:17:06Z
dc.date.issued1997
dc.identifier.citationYALCINKAYA C., Tuysuz B., SOMAY G., CENANI A., "Polydactyly and fetal hydantoin syndrome: An additional component of the syndrome?", CLINICAL GENETICS, cilt.51, sa.5, ss.343-345, 1997
dc.identifier.issn0009-9163
dc.identifier.othervv_1032021
dc.identifier.otherav_48f55b67-3354-4a4e-84bc-e70a27b9bd75
dc.identifier.urihttp://hdl.handle.net/20.500.12627/52500
dc.description.abstractWe report a 3-year-old girl with fetal hydantoin syndrome (FHS) whose mother had received phenytoin 600 mg/day throughout gestation. She had growth retardation, mental deficiency, craniofacial dysmorphism and iris colomobata specific to FHS. However, the patient did not have the distal phalangeal hypoplasia which is associated with FHS; instead, she had polydactyly of the sight foot. This seems to be the first FHS case in the literature with polydactyly.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTemel Bilimler
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.titlePolydactyly and fetal hydantoin syndrome: An additional component of the syndrome?
dc.typeMakale
dc.relation.journalCLINICAL GENETICS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume51
dc.identifier.issue5
dc.identifier.startpage343
dc.identifier.endpage345
dc.contributor.firstauthorID9954


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