Syndrome de Bartter et syndrome de Gitelman - Problèmes de santé infantiles - Manuels MSD pour le grand public
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Angelman syndrome is a rare genetic disorder that primarily affects the nervous system. It is caused by a mutation or deletion of genes on chromosome 15. It occurs in around 1 out of every 15,000 live births. Many doctors and nurses have never heard of this Syndrome and it is often misdiagnosed with Autism or cerebral palsy. Legacy’s first Pediatrician believed nothing was wrong with her and she was simply developmentally delayed. We switched Pediatricians when she was a year old (mother’s intui
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