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Unilateral tibial agenesia with preaxial polysyndactyly and renal disorder in two patients: a new syndrome?

dc.contributor.authorCENTEL, Tuncay
dc.contributor.authorUNGUR, Savaş
dc.contributor.authorBEKER, BD
dc.contributor.authorITER, O
dc.contributor.authorTuysuz, Beyhan
dc.date.accessioned2021-03-03T12:03:22Z
dc.date.available2021-03-03T12:03:22Z
dc.date.issued2001
dc.identifier.citationTuysuz B., BEKER B., CENTEL T., UNGUR S., ITER O., "Unilateral tibial agenesia with preaxial polysyndactyly and renal disorder in two patients: a new syndrome?", CLINICAL DYSMORPHOLOGY, cilt.10, sa.1, ss.37-40, 2001
dc.identifier.issn0962-8827
dc.identifier.othervv_1032021
dc.identifier.otherav_2b954e84-39b3-416c-b202-b9851f03a802
dc.identifier.urihttp://hdl.handle.net/20.500.12627/34048
dc.description.abstractLeft tibial agenesis, polysyndactyly with talipes equinovarus deformity and Grade IV vesicoureteral reflux of the right kidney are described in a 40-day-old male and an unrelated 1-month-old male, is also reported with right tibial agenesis, polysyndactyly with talipes equinovarus deformity and right kidney agenesis and left Grade V vesicoureteral reflux. No other pathology was recorded. Follow up at 1 year and 3 years, respectively, revealed normal motor and mental development. As this combination has been unpublished before, we believe that this a new syndrome. Clin Dysmorphol 10: 37-40 (C) 2001 Lippincott Williams & Wilkins.
dc.language.isoeng
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectGENETİK VE HAYAT
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıbbi Genetik
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.titleUnilateral tibial agenesia with preaxial polysyndactyly and renal disorder in two patients: a new syndrome?
dc.typeMakale
dc.relation.journalCLINICAL DYSMORPHOLOGY
dc.contributor.department, ,
dc.identifier.volume10
dc.identifier.issue1
dc.identifier.startpage37
dc.identifier.endpage40
dc.contributor.firstauthorID9889


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