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[Ito hypomelanosis: Four case reports]. / Hypomélanose d'Ito : à propos de 4 cas.
Sagna, S D; Mbonda, P; Ndiaye, M; Sow, A D; Basse, A M; Diop, M S; Diagne, N S; Diop, A G; Kane, A; Ndiaye, M M.
Afiliación
  • 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.
Arch Pediatr ; 23(10): 1050-1054, 2016 Oct.
Article en Fr | MEDLINE | ID: mdl-27642143
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Discapacidades del Desarrollo / Hipopigmentación / Epilepsia Límite: Female / Humans / Infant / Male Idioma: Fr Revista: Arch Pediatr Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Discapacidades del Desarrollo / Hipopigmentación / Epilepsia Límite: Female / Humans / Infant / Male Idioma: Fr Revista: Arch Pediatr Año: 2016 Tipo del documento: Article