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TOP 30 Pediatric genetic disorders in San Francisco, CA
9 results found
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UCSF Pediatric Lipid Clinic
The UCSF Pediatric Lipid Clinic, located at 2401 Shadelands Drive in Walnut Creek, California, provides comprehensive care for children with lipid disorders that affect their blood fat levels. Our world-class doctors specialize in diagnosing and managing genetic lipid disorders, as well as secondary causes like diabetes or kidney disease. Through a combination of diet modifications, exercise, and medication, we work to achieve normal lipid levels and prevent heart disease, stroke, and pancreatitis in our young patients. Established in 1971, our clinic has been at the forefront of research on lipid disorders and atherosclerosis, leading to valuable discoveries in the field. We offer training for residents, fellows, and practicing physicians in the diagnosis and management of lipid disorders. In addition, our facility provides a wide range of family-friendly amenities, including certified child life specialists, social workers, art therapy, music therapy, and educational programs to support children and families during their hospital stay.
UCSF Pediatric Hemophilia Treatment Center
The UCSF Pediatric Hemophilia Treatment Center, located at 1825 4th Street in San Francisco, California, is a world-class institution dedicated to providing exceptional care for children and families affected by hemophilia and other congenital blood-clotting disorders. Established in 1977, our center offers a comprehensive range of services including diagnosis, treatment, genetic screening, counseling, and education. Recognized by the Centers for Disease Control and Prevention as a specialized healthcare center for hemophilia, we are one of only 130 such centers in the country caring for both adult and pediatric patients. Our team of specialists, including hematologists, orthopedic surgeons, nurses, social workers, dentists, and physical therapists, work together to develop individualized care plans for our patients and their families.
UCSF Pediatric Disorders of Sex Development Clinic
The UCSF Pediatric Disorders of Sex Development Clinic in San Francisco, California, United States, is a world-class institution dedicated to providing expert care for babies and children with atypical development of the genitals and other sex characteristics. Our team of specialists in pediatric urology, pediatric endocrinology, genetics, child psychology, social work and nursing work together to create personalized treatment plans for each child. We follow national guidelines for the treatment of Differences in Sex Development (DSD) and offer comprehensive care that includes medical, social, and psychological support. Our clinic offers stress-free visits with accommodations for families, as well as a range of amenities to help families relax and take care of themselves while staying close to their child. Certified child life specialists, social workers, and art and music therapists are available to help children cope with illness, injury, and hospitalization. Our schoolroom services and individual learning programs ensure that children continue their education while hospitalized and are supported in their transition back to school.
UCSF Pediatric Medical Genetics and Genomics Clinic
The UCSF Pediatric Medical Genetics and Genomics Clinic, located at 744 52nd Street in Oakland, California, is a world-class institution dedicated to serving children who are at risk for or suspected of having a genetically based disorder. The clinic offers stress-free visits with accommodations for families, admission, discharge, and procedure prep all covered. The comprehensive team includes expert doctors in medical genetics and genetic counselors who work together to evaluate each child's medical records and family history to form accurate diagnoses and treatment plans. The clinic specializes in handling conditions ranging from common to the most rare genetic disorders. Parents typically visit the clinic because their child has a birth defect, developmental delays, learning differences, or a family history of a genetic condition. The clinic's approach includes considering the implications of a patient's health and genetic testing for the entire family, especially in cases where siblings may also be susceptible to genetic disorders. Children with known or suspected inborn errors of metabolism should be seen at the San Francisco clinic, where rare genetic disorders affecting the body's ability to turn food into energy are treated.
Sheva Tessler, MD - Stanford Medicine Children's Health
Sheva Tessler, MD at Stanford Medicine Children's Health located at 2100 Webster Street in San Francisco, California, is a dedicated pediatric doctor with a passion for helping children grow and thrive. Dr. Tessler's interest in pediatrics began at a young age, inspired by her father who was a pediatric cardiologist. She finds joy in interacting with children, appreciating their humor and resilience even in the face of illness. Dr. Tessler values the relationships she builds with both her young patients and their parents, drawing from her own experience as a parent to provide compassionate care. With a background in medicine from Pritzker School of Medicine University of Chicago and pediatric residency at UCSF Benioff Childrens Hospital, Dr. Tessler is well-equipped to address the medical needs of children while also offering support and reassurance to their families.
Dr. Ilona Frieden
Dr. Ilona Frieden is a renowned pediatric dermatologist located at 2380 Sutter Street, San Francisco, California. With over 35 years of experience, she specializes in treating children with a wide range of skin conditions, from common issues like eczema to rare genetic disorders. Dr. Frieden is also an expert in birthmarks, particularly those caused by abnormal blood vessels. She received her medical degree from UCSF and completed residencies in pediatrics and dermatology at the same institution. Dr. Frieden has been heavily involved in research and education, serving as an editor-in-chief of the journal Pediatric Dermatology and co-editing the textbook Neonatal and Infant Dermatology.
Anthony A. Portale, MD
Anthony A. Portale, MD is a world-class institution located at 1825 4th Street in San Francisco, California, United States. Specializing in pediatric kidney disorders, Dr. Portale and his team provide extraordinary care for children of all ages, from infants to young adults. With a focus on genetic diseases of the kidneys, bone and mineral metabolism, and acute kidney failure, Dr. Portale is a leading expert in his field. With funding from the National Institutes of Health, Dr. Portale's research focuses on genetic and acquired disorders of calcium, phosphorus, and vitamin D metabolism, as well as bone diseases in children. He has published over 80 articles in medical and scientific journals on these topics, showcasing his dedication to advancing the field of pediatric nephrology.
Dr. Tippi C. Mackenzie, MD
Dr. Tippi C. Mackenzie, MD, located in San Francisco, California, is a renowned institution specializing in pediatric surgery and fetal treatment. As a member of the Biomedical Sciences Program and Institute for Regeneration Medicine, Dr. Mackenzie focuses on innovative treatments such as stem cell transplantation in utero to address genetic diseases. With a background in general surgery and pediatric surgery fellowship, Dr. Mackenzie is dedicated to providing world-class care for children of all ages. The institution offers stress-free visits, expert care for a wide range of conditions, and cutting-edge therapies to give hope to families facing genetic disorders. Dr. Mackenzie's commitment to excellence and passion for improving outcomes make her a trusted provider in the field of pediatric health.
INVITAE
Invitae: Pioneering Genetic Testing for Healthier Futures Located at 1400 16th St, San Francisco, CA 94103, Invitae is a leading health-focused business dedicated to revolutionizing healthcare through comprehensive genetic testing. At Invitae, we believe that genetic testing can play a crucial role in guiding some of the most important health decisions. Our mission is to make genetic information accessible and actionable for everyone, integrating it seamlessly into routine healthcare.
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