Chromosome 10 Q26.1 Deletion Syndrome in a Patient Diagnosed Postnatal and the Mother Support for the Prevention of Postnatal Depression

In the last time due to the wide genetic methods of genetic mutation determination, a lot of rare syndromes were highlighted and described in detail so it could be made an anticipatory strategy for the child born with a known or even new genetic mutation. Many of those mutations are not inherited and not found in other family members so that it is important to elucidate for the child and family and for the future descendants the variety of evolution possibilities and to have in mind more medical scenarios after which the medical team can plan the interventions. Rehabilitation must start from first day of diagnosis and this must be integrated in a large vision of a multidisciplinary team and networks prepared for this. Planning helps doctors and families not to waste time and to give a stronger support to the mothers because they feel that their child can gain the abilities to have a good life and a good social integration. So, the courage of the mother is greater, and the mother will not confront with postpartum depression seeing the involvement and the competences of the medical team. Postpartum depression affects yearly more than 27,6% women worldwide. The way the team discussed and concluded about this rare entity the 10q26.1 mutation in a male patient decided the good outcome and the good care which the child has beneficiated.

Keywords: Chromosome 10q26.1; Children; Prevention; Postpartum depression; Genetic