Rare genetic conditions are challenging for the primary care provider to manage without proper guidelines. This clinical review is designed to assist the pediatrician, family physician, or internist in the primary care setting to manage the complexities of 16p11.2 deletion syndrome. A multidisciplinary medical home with the primary care provider leading the care and armed with up-to-date guidelines will prove most helpful to the rare genetic patient population. A special focus on technology to fill gaps in deficits, review of case studies on novel medical treatments, and involvement with the educational system for advocacy with an emphasis on celebrating diversity will serve the rare genetic syndrome population well.

Almost 4.9 percent of Indian medlinkchildren/medlink and adolescents suffer from impaired kidney function, reports a first nationwide survey. h2What

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Hospice Foundation of America Presents Webinar on 'Grieving Children and Adolescents: The Role of Internet Support'

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New York, NY : Oxford University Press, [2020]

The study showed that decreased care and increased control from the mother, high autonomy from father and increased rejection from both parents as risk factors associated with adolescent internet excessive use