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1.
Appl Neuropsychol Child ; 6(4): 327-334, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-27267212

RESUMO

Incontinentia Pigmenti (IP, OMIM#308300) is a rare X-linked genomic disorder (about 1,400 cases) that affects the neuroectodermal tissue and Central Nervous System (CNS). The objective of this study was to describe the cognitive-behavioural profile in children in order to plan a clinical intervention to improve their quality of life. A total of 14 girls (age range: from 1 year and 2 months to 12 years and 10 months) with IP and the IKBKG/NEMO gene deletion were submitted to a cognitive assessment including intelligence scales, language and visuo-spatial competence tests, learning ability tests, and a behavioural assessment. Five girls had severe to mild intellectual deficiencies and the remaining nine had a normal neurodevelopment. Four girls were of school age and two of these showed no intellectual disability, but had specific disabilities in calculation and arithmetic reasoning. This is the first description of the cognitive-behavioural profile in relation to developmental age. We stress the importance of an early assessment of learning abilities in individuals with IP without intellectual deficiencies to prevent the onset of any such deficit.


Assuntos
Comportamento Infantil/psicologia , Cognição/fisiologia , Incontinência Pigmentar/psicologia , Deficiência Intelectual/psicologia , Deficiências da Aprendizagem/psicologia , Qualidade de Vida/psicologia , Criança , Pré-Escolar , Feminino , Humanos , Incontinência Pigmentar/complicações , Lactente , Deficiência Intelectual/complicações , Aprendizagem/fisiologia , Deficiências da Aprendizagem/complicações , Testes Neuropsicológicos
2.
Pediatr Neurol ; 36(3): 199-201, 2007 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-17352958

RESUMO

Incontinentia pigmenti is an X-linked neurocutaneous disorder which is often lethal in males. Ectodermal tissues are involved, and affected females often have abnormalities of skin, teeth, hair, eyes, and the central nervous system. Central nervous system involvement ranges from none to multiple strokes, seizures, and mental retardation. Deletions in the nuclear factor kappa beta essential modulator gene at Xq28 are present in 70-80% of patients with incontinentia pigmenti. White matter abnormalities have been reported in females with significant neurologic involvement. This report describes a neurologically intact child with deletion positive incontinentia pigmenti with significant white matter involvement, broadening the scope of this finding in incontinentia pigmenti.


Assuntos
Encéfalo/patologia , Incontinência Pigmentar/patologia , Criança , Feminino , Humanos , Quinase I-kappa B/genética , Incontinência Pigmentar/genética , Incontinência Pigmentar/psicologia
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