Penile agenesis and clavicular anomaly in a child with an oral facial digital syndrome

dc.authorid0000-0001-8142-8794en_US
dc.contributor.authorYıldırım, Serkan
dc.contributor.authorAkan, Mithat
dc.contributor.authorDeviren, Ayhan
dc.contributor.authorAköz, Tayfun
dc.date.accessioned2024-07-12T21:03:01Z
dc.date.available2024-07-12T21:03:01Z
dc.date.issued2002en_US
dc.departmentFakülteler, Tıp Fakültesien_US
dc.description.abstractOral facial digital syndromes (OFDS) comprise a heterogeneous group of disorders characterized by anomalies of the face (cleft lip and palate), the tongue (bifid or lobulated tongue with hamartomas) and the digits (brachydactyly, polydactyly, syndactyly, clinodactyly). The classification includes nine different types (Toriello, 1993) and two further possible types have been added (Figuera et al., 1993; Camera et al., 1994). Although clinical variability in OFDS may reflect genetic heterogeneity, there is some overlap between these groups, and misdiagnosis may account for some of the variability or overlapping manifestations. All of the subgroups apart from type I (X-linked dominant) and type VIII (X-linked recessive) appear to be autosomal recessive traits.en_US
dc.identifier.citationYıldırım, S., Akan, M., Deviren, A. ve Aköz, T. (2002). Penile agenesis and clavicular anomaly in a child with an oral facial digital syndrome. Clinical Dysmorphology. 11(1), s. 29-32.en_US
dc.identifier.endpage32en_US
dc.identifier.issn1473-5717
dc.identifier.issue1en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage29en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12415/3615
dc.identifier.volume11en_US
dc.language.isoenen_US
dc.publisherWolters Kluwer Healthen_US
dc.relation.ispartofClinical Dysmorphologyen_US
dc.relation.publicationcategoryUluslararası Hakemli Dergide Makale - Kurum Öğretim Elemanıen_US
dc.rightsCC0 1.0 Universal*
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.snmzKY00529
dc.titlePenile agenesis and clavicular anomaly in a child with an oral facial digital syndromeen_US
dc.typeArticle
dspace.entity.typePublication

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