Snijder-Blok Campaeu Syndrom CHD3 Mutation
Geplaatst: 28 mei 2020, 07:19
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
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