References of "Maton, P"
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See detailDiagnostic pitfall in antenatal manifestations of CPT II deficiency.
BOEMER, François ULg; DEBERG, Michelle ULg; SCHOOS, Roland ULg et al

in Clinical genetics (2015)

Carnitine palmitoyltransferase II (CPT2) deficiency is a rare inborn error of mitochondrial fatty acid metabolism associated with various phenotypes. Whereas most patients present with postnatal signs of ... [more ▼]

Carnitine palmitoyltransferase II (CPT2) deficiency is a rare inborn error of mitochondrial fatty acid metabolism associated with various phenotypes. Whereas most patients present with postnatal signs of energetic failure affecting muscle and liver, a small subset of patients presents antenatal malformations including brain dysgenesis and neuronal migration defects. Here, we report recurrence of severe cerebral dysgenesis with Dandy-Walker malformation in three successive pregnancies and review previously reported antenatal cases. Interestingly, we also report that acylcarnitines profile, tested retrospectively on the amniotic fluid of last pregnancy, was not sensitive enough to allow reliable prenatal diagnosis of CPT2 deficiency. Finally, because fetuses affected by severe cerebral malformations are frequently aborted, CPT2 deficiency may be underestimated and fatty acid oxidation disorders should be considered when faced with a fetus with Dandy-Walker anomaly or another brain dysgenesis. [less ▲]

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See detailCathéter épicutanéo-cave double voie versus simple voie: une étude randomisée chez le nouveau-né prémature
Marion, W.; Battisti, Oreste ULg; Anthopoulou, N. et al

Conference (2007)

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See detailPseudo-Bartter syndrome in a pregnant mother and her fetus
Mathot, Michel ULg; Maton, P.; Henrion, Elisabeth ULg et al

in Pediatric Nephrology (2006), 21(7), 1037-1040

Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrome but without primary renal tubule abnormalities. We relate the case of a premature baby presenting at ... [more ▼]

Pseudo-Bartter syndrome presents the same clinical and biological characteristics as Bartter syndrome but without primary renal tubule abnormalities. We relate the case of a premature baby presenting at birth with severe hypokalemic metabolic alkalosis associated with hyponatremia and hypochloremia. Maternal blood at the time of delivery showed the same electrolyte perturbations. The baby's mother had suffered from anorexia and vomiting during pregnancy. A few weeks after birth the baby's blood abnormalities had almost returned to normal. Chloride depletion is at the origin of both maternal and fetal hypokalemic alkalosis. [less ▲]

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See detailDo antenatal steroids affect postnatal head growth ?
Battisti, Oreste ULg; Maton, P.; François, A. et al

Conference (2002)

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See detailThe acquired brain injuries in the term and preterm babies: an update on their pathophysiology
Battisti, Oreste ULg; Adant-François, A.; Scalais, E. et al

in Journal du Pédiatre Belge (2001), 3

Detailed reference viewed: 35 (7 ULg)