December, 21 1998
I'm pediatritian working in a portuguese hospital. In my general pediatric
consultation we have a boy suffering from moderate mental delay, deafness
and branchial clefts. We think he can be considered number 3133 in
classification(Branchio-oto-renal) and we had found in his family similar cases until 4th generation.
Is it possible to know if there are any genetic and molecular studies in this particular situation?
Thank you very much for your help