11 research outputs found

    Congenital muscular dystrophy and epileptic syndromes in infancy and childhood.

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    Distrofia muscolare congenita associata a ritardo mentale, cataratta e criptorchidismo

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    Neuropatia ipomielinizzante congenita: presentazione di un caso clinico.

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    DIAGNOSTIC PROBLEMS IN CONGENITAL MYOTONIC DYSTROPHY.

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    Supplementary Material for: Clinical and Molecular Cytogenetic Characterization of a de novo Interstitial 1p31.1p31.3 Deletion in a Boy with Moderate Intellectual Disability and Severe Language Impairment

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    Interstitial 1p deletions are rare events. Very few cases of 1p31.1p31.3 deletions characterized by variable phenotypes have been reported. No clear genotype-phenotype correlation has been determined yet. We present a child with a de novo interstitial 1p31.1p31.3 deletion, identified by array CGH, associated with intellectual disability and severe language impairment. The deleted region contains 20 OMIM genes, but we focused on <i>GADD45A</i> (MIM 126335; growth arrest- and DNA damage-inducible gene), <i>LRRC7</i> (MIM 614453; leucine-rich repeat-containing protein 7), and <i>NEGR1</i> (MIM 613173; neuronal growth regulator 1). We discuss whether these genes play a role in determining the phenotype of our patient in order to investigate the possibility of a genotype-phenotype correlation

    Metabolic and genetic risk factors for migraine in children

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    Abstract Migraine can induce ischaemic stroke, and is considered an independent risk factor for stroke in the young. To date, the nature of the link between migraine and stroke is essentially unknown. Forty-five children were studied. Homocysteine levels (fasting and post methionine load), vitamin B12 and plasma folate levels, factor V Leiden, factor II G20210A, methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C mutations were examined. Compared with controls, patients with migraine had higher levels of post-methionine load homocysteine values (19.5 +/- 4.9 vs. 16.9 +/- 1.9; P = 0.025) and significantly lower folate levels (5.8 +/- 2.6 vs. 7.5 +/- 2.1; P = 0.002). We found a trend toward an increased risk of migraine in subjects carrying a homozygous mutant genotype for MTHFR C677T and MTHFR A1298C polymorphisms. Genetic prothrombotic conditions do not seem to be related to migraine in the young, whereas the biochemical differences between migrainous patients and controls are an appealing topic for further investigation

    Distrofia muscolare congenita con e senza ritardo mentale.

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