Pediatric Genetics

Understanding and managing inherited disorders in children

To schedule an appointment or refer a patient, please call (602) 914-1520

Some children are born with differences in body chemistry or structure, or brain development that can lead to problems with long term health, mental and physical development, school performance, and/or social interactions. Pediatric geneticists identify the causes and natural history of these disorders through tests, assessments, and treatments and can help you manage your child’s condition.

These pediatric genetics specialists also help determine if the condition is hereditary and offer testing to family members who may be at risk for having children with similar problems. Some pediatric genetic disorders include:

Birth defects or conditions with more than one birth defect
Conditions that can cause disabilities like fetal alcohol syndrome or fragile X syndrome
Inborn errors of metabolism
Familial or hereditary problems such as congenital heart disease (CHD)
Short or tall stature

DMG CRS pediatric geneticists help families and children understand the genetic considerations and treatment options relating to an inherited disorder or condition. In partnership with appropriate pediatric specialists based on your child’s specific condition, our pediatric genetics experts will help you understand:

Complex issues involved
Risk factors
Chances of recurrence
How to cope
Treatment options and recommendations

DMG CRS genetic specialists provide information in an easy-to-understand manner; are an available resource for you and your family long after any procedures or tests are completed; and offer emotional and psychological support.

Por qué una niña necesitaría ver a una especialista genética

Christine Umandap, MD, genetista pediátrica, habla sobre cómo puede ayudar a los niños en DMG CRS. Descubra por qué puede ser importante consultar a un especialista en genética.