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The Tuberous Sclerosis Complex Clinic at the Virginia Neurology Center in Fairfax Virginia is under the medical direction of Dr. William McClintock and meets quarterly in January, April, July, and October. Each clinic begins at 9:00 a.m. and runs until approximately 1:00 p.m. Several families attend each session to receive consultation and for the purpose of data collection. Follow-ups every two to three years will be critical for the individuals as well as for our database which needs to reflect developments among large group of patients over time. This self-supported clinic approved by NTSA was started in January 1994. The clinic is modeled after other clinics that have been functioning very successfully in the United States and in Great Britain for several years. We are very proud of the efforts of the physicians, the volunteers and the efforts of the families and friends that donate time and funds to keep the clinic operating. At the clinic, we well review the questionnaire that families are asked to fill out with Dr. McClintock and Dr. David Daigh. Dr. McClintock will also perform a neurological examination, and may be assisted by a medical student or resident/intern. An important additional function of the clinic is to teach young physicians and medical students about tuberous sclerosis, so they may recognize cases when they come across one. Dr. Robert Silverman, a dermatologist, and Dr. Susan Black, a geneticist, are also available during the clinic to answer questions in their respective areas. Dr. Silverman will be involved in screening parents and siblings for white spots and other skin conditions in an effort to verify diagnosis. Dr. Black will be available to address the genetic aspects of tuberous sclerosis. The newest additions to our clinic are Dr. Micheal Medlock a neurosurgeon, who will be available for consultation on aspects of epilepsy surgery and Dr. Phillip Pearl, a pediatric neurologist who practices with Dr. McClintock. We would value any suggestions or requests you have for additional specialists to become involved as the clinic develops. Washington Metro Council members will be present at the clinic to help answer questions and to provide refreshments. We all have found that the conversation and experiences exchanged by the families and friends of tuberous sclerosis patients to be extremely valuable to the participants. We will hold group discussion with the physicians at the end of the clinic, time permitting. You can directly register through this site. Click here to find out what some families thought about their experience with the clinic or read A Day at the Clinic in Newsletter Archives. |
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