Angelman-Syndrom

Wenn der Sohn ein Leben lang Kleinkind bleibt

| Lesedauer: 6 Minuten
Sibylle Haberstumpf
Der fünfjährige Philip hat das Angelman-Syndrom. Seine Eltern Regina Heese und Mirko Seidel aus Petershagen wollen über den seltenen Gendefekt aufklären.

Der fünfjährige Philip hat das Angelman-Syndrom. Seine Eltern Regina Heese und Mirko Seidel aus Petershagen wollen über den seltenen Gendefekt aufklären.

Foto: Maurizio Gambarini / FUNKE Foto Services

Der 15. Februar ist dem Angelman-Syndrom gewidmet. Die Eltern eines Fünfjährigen erzählen von der Krankheit.

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Geistig wird Philip sein Leben lang ein Kleinkind bleiben

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Schauspieler Jürgen Vogel ist Schirmherr des Vereins

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