Arthrogryposis Multiplex Congenita: Case Report
Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome. Prevalence is determined to be 1 in 3000 deliveries. Although it is autosomal recessively inherited, sporadic cases have also been...
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| Format: | Article |
| Language: | English |
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Medical Network
2013-12-01
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| Series: | Gynecology Obstetrics & Reproductive Medicine |
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| Online Access: | https://gorm.com.tr/index.php/GORM/article/view/214 |
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| author | Ayla Aktulay Saliha Sağnıç Özlem Moraloğlu Tekin Yaprak Engin Üstün Elif Gül Yapar Eyi Leyla Mollamahmutoğlu |
| author_facet | Ayla Aktulay Saliha Sağnıç Özlem Moraloğlu Tekin Yaprak Engin Üstün Elif Gül Yapar Eyi Leyla Mollamahmutoğlu |
| author_sort | Ayla Aktulay |
| collection | DOAJ |
| description |
Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome. Prevalence is determined to be 1 in 3000 deliveries. Although it is autosomal recessively inherited, sporadic cases have also been reported. Prenatal diagnosis of AMC is difficult. Here we report a case with a diagnosis of AMC not diagnosed during antenatal follow-up.
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| format | Article |
| id | doaj-art-0530da8da89f42cf8c20961ae690003e |
| institution | Kabale University |
| issn | 1300-4751 2602-4918 |
| language | English |
| publishDate | 2013-12-01 |
| publisher | Medical Network |
| record_format | Article |
| series | Gynecology Obstetrics & Reproductive Medicine |
| spelling | doaj-art-0530da8da89f42cf8c20961ae690003e2025-02-11T21:22:13ZengMedical NetworkGynecology Obstetrics & Reproductive Medicine1300-47512602-49182013-12-01193152Arthrogryposis Multiplex Congenita: Case ReportAyla Aktulay0Saliha Sağnıç1Özlem Moraloğlu Tekin2Yaprak Engin Üstün3Elif Gül Yapar Eyi4Leyla Mollamahmutoğlu5Zekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, AnkaraZekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, AnkaraZekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, AnkaraZekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, AnkaraZekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, AnkaraZekai Tahir Burak Kadın Sağlığı Eğitim ve Araştırma Hastanesi, Ankara Arthrogryposis multiplex congenita (AMC), characterized by multiple congenital joint contractures due to decreased fetal movements, is a non-progressive rare syndrome. Prevalence is determined to be 1 in 3000 deliveries. Although it is autosomal recessively inherited, sporadic cases have also been reported. Prenatal diagnosis of AMC is difficult. Here we report a case with a diagnosis of AMC not diagnosed during antenatal follow-up. https://gorm.com.tr/index.php/GORM/article/view/214ArthrogryposisMultiplexCongenita |
| spellingShingle | Ayla Aktulay Saliha Sağnıç Özlem Moraloğlu Tekin Yaprak Engin Üstün Elif Gül Yapar Eyi Leyla Mollamahmutoğlu Arthrogryposis Multiplex Congenita: Case Report Gynecology Obstetrics & Reproductive Medicine Arthrogryposis Multiplex Congenita |
| title | Arthrogryposis Multiplex Congenita: Case Report |
| title_full | Arthrogryposis Multiplex Congenita: Case Report |
| title_fullStr | Arthrogryposis Multiplex Congenita: Case Report |
| title_full_unstemmed | Arthrogryposis Multiplex Congenita: Case Report |
| title_short | Arthrogryposis Multiplex Congenita: Case Report |
| title_sort | arthrogryposis multiplex congenita case report |
| topic | Arthrogryposis Multiplex Congenita |
| url | https://gorm.com.tr/index.php/GORM/article/view/214 |
| work_keys_str_mv | AT aylaaktulay arthrogryposismultiplexcongenitacasereport AT salihasagnıc arthrogryposismultiplexcongenitacasereport AT ozlemmoraloglutekin arthrogryposismultiplexcongenitacasereport AT yaprakenginustun arthrogryposismultiplexcongenitacasereport AT elifgulyapareyi arthrogryposismultiplexcongenitacasereport AT leylamollamahmutoglu arthrogryposismultiplexcongenitacasereport |