July, 12 1999

I've had a request for information of similar cases from a mother of a 3 year old girl with karyotype : 46,XX,del(7)(pter->q22.3::q31.1->qter) de novo. This mother seeks addresses of families or support groups of rare chromosome abnormalities, in the hope that families with children with similar deletion breakpoints might be able to communicate.

Many thanks.