Pediatric Genetics
Meet the Care Team
Conditions We Treat
Pediatric achondroplasia (dwarfism)
Hypohidrotic ectodermal dysplasia
Pediatric Marfan syndrome (MFS)
McCune-Albright syndrome (MAS)
Pediatric metabolic diseases
Congenital chromosomal anomalies
Down syndrome in children
Treacher Collins syndrome
Yunis-Varon syndrome
Developmental delays in children
Pediatric autism spectrum disorder (ASD)
Fragile X syndrome (FXS) in children
Rett syndrome in children
Pediatric Ehlers-Danlos syndrome (EDS or elastic skin)
Pediatric short stature
Klinefelter syndrome (KS)
Pediatric and adolescent Turner syndrome (TS)
Congenital Anomalies
Chromosome Deletion
Chromosome Duplication
Chromosome Rearrangement Syndromes
Connective Tissue Disorders
Hearing Loss
Parents Who Are Related to Each Other
Positive Genetic Screening Tests (Carrier, Prenatal and Newborn)
Unexplained Episodic Illnesses
Unusual Physical Features With Poor Growth and Development
Unexplained Intellectual Disability
Vision Loss
More Details
Department Overview
Every new patient who comes to our clinic is seen by a medical geneticist and a genetic counselor. Our physicians are all certified by the American Board of Medical Genetics and have extensive clinical experience. Every genetic counselor has a master’s degree in genetic counseling and is board certified or eligible. Experienced social workers are available by request, or when the need arises.
Medical Genetics offers evaluation and testing, information about specific genetic diseases, family history analysis, and chromosomal, metabolic and DNA analysis for the diagnosis of diseases. Counselors can assist with genetic counseling and discussions of options for having children. Social workers can link the family to other medical specialists as needed, as well as community resources and support groups.
Our genetics team are experts in:
Single-gene disorders, where a mutation affects one gene. Sickle cell anemia is an example.
Chromosomal disorders, where chromosomes (or parts of chromosomes) are missing or changed.
Complex disorders, with mutations in two or more genes. Often lifestyle and environment also play a role.
Services
Evaluation and testing for children with known or suspected inborn errors of metabolism
Prenatal screening, newborn screening and carrier screening
Interpretation of genetic test results
Family history analysis and genetic counseling to discuss reproductive options as pertains to inborn errors of metabolism
Education about specific inborn errors of metabolism
Comprehensive case management with referral to medical specialists, community resources and support groups
Consultation regarding abnormal newborn screening and metabolic testing results
Resources
Have questions about what to expect at your appointment? Read our frequently asked questions (FAQs).
Genetic Home Reference - Information about genetic conditions, as well as helpful definitions.
Navigate Life Texas - Information about resources available to Texas families who have a child with special needs.
National Organization for Rare Diseases (NORD) 800-999-6973 - Support for individuals with rare diseases by advocating and funding research, education, and networking among service providers
Children's Health Financial Counseling 214-456-8670
In the Children’s Health℠ Genetics clinic, we see children up to age 19 who have a known or suspected genetic condition. Genes are the building blocks of heredity that hold DNA, the instructions for making proteins. Proteins do most of the work in cells by moving molecules to where they are needed, building structures, breaking down toxins and doing general clean up and maintenance work around the body. Sometimes there is a mutation or a change in a gene or genes. This effects the gene's instructions for making a protein. If the protein is missing or not working properly, this causes a medical condition known as a genetic disorder.