Ring chromosome 14 syndrome presenting with intractable epilepsy: a case report
Ring chromosome 14 syndrome is a rare genetic disorder. Typically, children with this syndrome have distinct facial features, development delay, microcephaly, seizures, ocular abnormalities, and recurrent respiratory infections. Epilepsy associated with ring chromosome 14 generally shows intr...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Hacettepe University Institute of Child Health
2013-10-01
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| Σειρά: | The Turkish Journal of Pediatrics |
| Διαθέσιμο Online: | https://turkjpediatr.org/article/view/1552 |
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