Long-term follow-up of neurological manifestations in a boy with incontinentia pigmenti

European Journal of Pediatrics

Volumn 172, Issue 9, 2013, Pages 1259-1262

  Margari, Lucia ^a   Lamanna, Anna Linda ^a   Buttiglione, Maura ^a   Craig, Francesco ^a   Petruzzelli, Maria G ^a   Terenzio, Vanessa ^a  

^a UNIVERSITY OF BARI   (Italy)

Author keywords

Epilepsy; Geneticmosaicism; Incontinentia pigmenti; Lethal gene; Neurologicalmanifestations; X linked

Indexed keywords

ETIRACETAM; VALPROIC ACID;

ARTICLE; CASE REPORT; CEREBELLAR ATAXIA; CHILD; CHROMOSOME XQ; CONGENITAL MALFORMATION; ELECTROENCEPHALOGRAPHY; EPILEPSY; FOLLOW UP; HUMAN; INCONTINENTIA PIGMENTI; MALE; MEDICAL HISTORY; NEUROLOGIC DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHOOL CHILD;

CEREBELLAR ATAXIA; CHILD; EPILEPSY; GENETIC MARKERS; GENETIC TESTING; HUMANS; I-KAPPA B KINASE; INCONTINENTIA PIGMENTI; MALE; MOSAICISM;

EID: 84892742644     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-013-2021-8     Document Type: Article

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