La maladie de Hirschsprungs est une affection congénitale qui empêche les personnes - généralement les nouveau-nés et les jeunes enfants - d'évacuer leurs selles. Voici un guide du médecin sur cette maladie, y compris les symptômes et le traitement.
Dans le cas du gastroschisis, les intestins et autres organes internes passent par un trou dans la paroi du ventre et apparaissent à l'extérieur du corps du bébé.
Que vous disent la température, les fréquences cardiaque et respiratoire et la tension artérielle de votre enfant ? Apprenez ce qui est normal ou préoccupant.
Votre bébé n'a qu'un jour et il subit déjà son premier test. Cet important test sanguin permet de détecter des maladies rares, dont la PCU. Voici ce que vous devez savoir.
La galactosémie est une maladie génétique rare qui empêche les bébés de traiter le galactose, un sucre important dans le lait maternel. Bien que la maladie puisse causer de nombreux problèmes, elle est facile à diagnostiquer et à traiter.
Il est difficile de voir son enfant faire une crise. Mais lorsque cela se produit en même temps qu'une fièvre, ce n'est généralement pas dangereux. Le médecin vous en dira plus sur les crises fébriles et sur les mesures à prendre pour aider votre enfant.
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