Genetic Disorders & Pediatric Genomic DNA | Cleveland Clinic

Overview

Learning that your child may have a genetic condition can be a frightening and confusing time. We are available to help in finding a diagnosis for your child, as well as to explain genetic testing options and results. Our goal is to support you and your family with your emotional as well as your medical needs. Our pediatric specialty clinics include:

• Pediatric Hearing Management Clinic (hearing loss).
• Neurofibromatosis Clinic (NF1, NF2).
• Neurogenetics & Metabolism Clinic (autism, lysosomal disorders, mitchondrial disorders).

Scheduling an Appointment

Prior to requesting an appointment, you will need to obtain a referral from your physician. If you are a patient outside Cleveland Clinic, please have your physician complete a referral form and fax to 216.445.6935. Learn more about how to prepare for your appointment and download the Patient Referral form .

Who Should Be Seen

You should consider having your child evaluated by a genetics expert if they have a family and/or personal history of the following: Developmental delay or learning difficulties. Birth defects, such as spina bifida, cleft palate, brain malformations, heart defects, etc. Unusual physical features. Hearing loss. Abnormal growth. Muscular dystrophy or other neuromuscular disorder. An abnormal genetic test result. A known or suspected genetic condition. A family history of a genetic condition. Parents interested in learning about recurrence risks. Contact your child's primary care provider or the Center for Personalized Genetic Healthcare (CPGH) to discuss whether a genetic counseling evaluation is appropriate for your child.