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dc.contributor.authorAlkanat, Funda
dc.contributor.authorSayar, Ceyhan
dc.contributor.authorSarak, Kader
dc.contributor.authorŞen, Aysel
dc.contributor.authorToksoy, Güven
dc.contributor.authorYardımcı, Tülay
dc.date.accessioned2021-03-04T10:34:54Z
dc.date.available2021-03-04T10:34:54Z
dc.identifier.citationYardımcı T., Sayar C., Toksoy G., Sarak K., Alkanat F., Şen A., "A case report: Amyoplasia ”Classical artrogryposis”", V. Ulusal Tıbbi Genetik Kongresi, Konya, Türkiye, 9 - 12 Ekim 2002, cilt.1, sa.1, ss.9
dc.identifier.othervv_1032021
dc.identifier.otherav_6df70f57-de10-46b2-a3be-160d33575bb8
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75937
dc.description.abstractAmyoplasia is a ran~. sporadic condition characterized by different degrees of maldevelopment ofthe skeletal muscks, which are replaced by fibrous and fatty tissue. In this report we present a caseof generalized amyoplasia diagnosed clinically at 12th day of life. The most striking findingswere a row1d face \:vi th a mid-line haemangioma, mi Id micrognathia, symmetrical contractures onupper and lower extremities, a firm fibrous band on left elbow, right humerus fracture as acomplication of sectio delivery due to breech presentation, dislocated hips with equinovarus feetand lack of labium major. Photos and X-ray graphies were taken.Ultrasonographic evaluationrevealed no visceral abnormalities. Eye examination was normal. Cranial CAT scan andelectromyography for muscle response were ordered. Chromosome analysis revealed 46 XX~aryotyp~. The c~se was send to University Hospital for further orthopedic and rehabilitativemtervent1ons. This report suggests that generalized amyoplasia could be a common cause ofsevere forms of multiple congenitalcontr~ctures but once it is diagnosed with early orthopedic and rehabilitative therapy thefunctional outcome can be excellent.
dc.language.isotur
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectMoleküler Biyoloji ve Genetik
dc.subjectTIP, GENEL & İÇECEK
dc.subjectPEDİATRİ
dc.subjectGENETİK VE HAYAT
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectÇocuk Sağlığı ve Hastalıkları
dc.subjectPediatrik Nöroloji
dc.subjectTıbbi Genetik
dc.titleA case report: Amyoplasia ”Classical artrogryposis”
dc.typeBildiri
dc.contributor.department, ,
dc.identifier.volume1
dc.contributor.firstauthorID1041675


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