dc.contributor.author | Alkanat, Funda | |
dc.contributor.author | Sayar, Ceyhan | |
dc.contributor.author | Sarak, Kader | |
dc.contributor.author | Şen, Aysel | |
dc.contributor.author | Toksoy, Güven | |
dc.contributor.author | Yardımcı, Tülay | |
dc.date.accessioned | 2021-03-04T10:34:54Z | |
dc.date.available | 2021-03-04T10:34:54Z | |
dc.identifier.citation | Yardımcı 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.other | vv_1032021 | |
dc.identifier.other | av_6df70f57-de10-46b2-a3be-160d33575bb8 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/75937 | |
dc.description.abstract | Amyoplasia 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.iso | tur | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | Klinik Tıp | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | TIP, GENEL & İÇECEK | |
dc.subject | PEDİATRİ | |
dc.subject | GENETİK VE HAYAT | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | Çocuk Sağlığı ve Hastalıkları | |
dc.subject | Pediatrik Nöroloji | |
dc.subject | Tıbbi Genetik | |
dc.title | A case report: Amyoplasia ”Classical artrogryposis” | |
dc.type | Bildiri | |
dc.contributor.department | , , | |
dc.identifier.volume | 1 | |
dc.contributor.firstauthorID | 1041675 | |