دورية أكاديمية
[Ito hypomelanosis: Four case reports].
| العنوان: | [Ito hypomelanosis: Four case reports]. |
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| عنوان ترانسليتريتد: | Hypomélanose d’Ito : à propos de 4 cas. |
| المؤلفون: | Sagna SD; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Mbonda P; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal; Service de neurologie, Yaoundé, Cameroun., Ndiaye M; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal. Electronic address: ngouille@hotmail.com., Sow AD; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Basse AM; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Diop MS; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Diagne NS; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Diop AG; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal., Kane A; Unité de dermatologie, HEAR, Dakar, Sénégal., Ndiaye MM; Service de neurologie, CHU Fann, BP 5035, Dakar, Sénégal. |
| المصدر: | Archives de pediatrie : organe officiel de la Societe francaise de pediatrie [Arch Pediatr] 2016 Oct; Vol. 23 (10), pp. 1050-1054. Date of Electronic Publication: 2016 Sep 15. |
| نوع المنشور: | Case Reports; Journal Article |
| اللغة: | French |
| بيانات الدورية: | Publisher: Elsevier Country of Publication: France NLM ID: 9421356 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1769-664X (Electronic) Linking ISSN: 0929693X NLM ISO Abbreviation: Arch Pediatr Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: Paris : Elsevier Original Publication: Paris : Editions Scientifiques Elsevier, 1994- |
| مواضيع طبية MeSH: | Developmental Disabilities/*complications , Epilepsy/*complications , Hypopigmentation/*complications, Atrophy/diagnostic imaging ; Brain/pathology ; Electroencephalography ; Female ; Humans ; Infant ; Male |
| مستخلص: | Ito hypomelanosis is a rare neurocutaneous condition. We report on four observations in infants aged between 8 and 20 months. They all presented with epilepsy, psychomotor delay, and diffuse hypomelanosis. The electroencephalograms showed diffuse irritative abnormalities. Brain imaging was normal in two infants and showed hemispheric atrophy in another case. Despite antiepileptic treatment and physical therapy, no significant progression was noted and all children continued to have drug-resistant epilepsy and psychomotor delay. (Copyright © 2016 Elsevier Masson SAS. All rights reserved.) |
| تواريخ الأحداث: | Date Created: 20160920 Date Completed: 20170418 Latest Revision: 20170418 |
| رمز التحديث: | 20221213 |
| DOI: | 10.1016/j.arcped.2016.06.021 |
| PMID: | 27642143 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder | تدمد: | 1769-664X |
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| DOI: | 10.1016/j.arcped.2016.06.021 |