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Snijder-Blok Campaeu Syndrom CHD3 Mutation

Geplaatst: 28 mei 2020, 07:19
door Taria
Hello from Germany!

My son Jaron (9 years old) has in addition to a distinctive Pierre Robin Sequence, a lot of other disbilities with unknown reason. After years of searching, a human geneticist diagnosed the „Snijder-Blok Campaeu Syndrom“ / CHD3 mutation.

I´m looking for contact for an exchange with other affected people.

I have so many questions and would be happy to hear from you.

Thank you in advance.


With best regards

Anke Potzel

Re: Snijder-Blok Campaeu Syndrom CHD3 Mutation

Geplaatst: 07 dec 2022, 23:37
door Spain
Hola Anke.
Recientemente mi hijo de 7 años ha sido diagnosticado con síndrome Snijders blok campeau.
Me encantaría poder intercambiar aspectos que hemos visto en nuestros hijos y cosas que vamos descubriendo.
Mi nombre es Arancha :-)
Un abrazo

Re: Snijder-Blok Campaeu Syndrom CHD3 Mutation

Geplaatst: 19 jan 2024, 11:08
door franciscarrasco
Hope that your son will be healthy.