Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fatma Kamoun Feki"'
Autor:
Chahnez Charfi Triki, Salma Zouari Mallouli, Marwa Ben Jdila, Mariem Ben Said, Fatma Kamoun Feki, Sarah Weckhuysen, Sabeur Masmoudi, Faiza Fakhfakh
Publikováno v:
Epilepsia Open, Vol 9, Iss 3, Pp 906-917 (2024)
Abstract Objective Mutations in the cyclin‐dependent kinase‐like 5 gene (CDKL5) are associated with a wide spectrum of clinical presentations. Early‐onset epileptic encephalopathy (EOEE) is the most recognized phenotype. Here we describe phenot
Externí odkaz:
https://doaj.org/article/c640a6965bed4f77a3a6d07f66909886
Autor:
Salma Zouari Mallouli, Sahar Najjar, Fatma Kamoun Feki, Olfa Jallouli, Sihem Ben Nsir, Wafa Bouchaala, Matilde Leonardi, Chahnez Charfi Triki
Publikováno v:
International Journal of Public Health Science (IJPHS). 12:239
To record the experience of caregivers for neurologically impaired children during the lockdown periods. Data from 286 children's caregivers were collected through an administered questionnaire to record: access to care services during the lockdown p
Publikováno v:
Multiple sclerosis and related disorders. 56
Introduction The yearly incidence of Acute Demyelinating Syndromes (ADS) in a multiethnic cohort of children published by Langer-Gould and al in 2011 was estimated at about 1.66 per 100,000. Nevertheless, the real incidence for these disorders is sti
Autor:
Zeineb Mnif, Basma Ayadi, Wafa Bouchaala, Siham Ben Nsir, Chahnez Triki, Fatma Kamoun Feki, Mounir Ben Jemaa
Publikováno v:
Journal of Pediatric Neurology. 18:114-117
Central nervous system (CNS) BCGitis is a rare but a very severe complication of the Bacille Calmette–Guerin (BCG) vaccine. It could be a diagnostic challenge that may lead to a delay in treatment. A 5-month-old boy presented with infantile spasms,
Autor:
Fatma, Kamoun Feki, Norhene, Fendri Kriaa, Dalinda, Kolsi, Ahmed, Rabai, Faiza, Fakhfakh, Chahnez, Charfi Triki
Publikováno v:
La Tunisie medicale. 97(4)
FS are the most benign occasional seizures in childhood. Little is known about the long term follow up. Aim: To describe a long term follow-up of FS in Tunisian families.Field study was conducted for 30 patients with FS. We analyzed clinical phenotyp
Publikováno v:
Journal of Pediatric Epilepsy. :021-023
Juvenile Huntington's disease (JHD) shares many general clinical features with the adult form. One important difference is that JHD patients experience more epileptic manifestations, sometimes difficult to control. We describe an atypical clinical pi
Publikováno v:
La Tunisie medicale. 96(8-9)
The identification of the epileptic syndrome is a challenge particularly in childhood epilepsies. In fact, the diagnosis may need several years to be fulfilled.Our patient presented at the age of 3 years 6 months atypical absence. His electroencephal