Genetic Counseling Center - Knoxville, TNKnoxville Medical Geneticist Doctors for Genetic CounselingType of Physician: Medical Geneticist What is a Medical Geneticist? A certification by the Board of Medical Genetics; practitioners work in association with a medical specialist, are affiliated with a clinical genetics program, or serve as a consultant to medical and dental specialists. Specialty: Genetics, Medical Common Name: Medical Geneticist Doctors in Knoxville * University Tennessee Genetics  University Tennessee Genetics  University Tennessee Genetics Knoxville, TennesseeUpcoming Local Events2013-05-25
2013-06-03
2013-06-05
2013-06-07
2013-06-08
2013-07-04
2013-07-04
2013-09-15
2013-10-12
2013-10-12
Genetic CounselingWhat are genetic professionals and what do they do?Genetics professionals are health care professionals with specialized degrees and experience in medical... Other Related Genetic Counseling ArticlesEmergency Contact for Knoxville
Nearby Knoxville Hospitals *Fort Sanders Regional Med Ctr Select Specialty Hospital East Tennessee Children's Hosp  University Of Tennessee Med Ctr  Physicians Regional Med Ctr  Select Specialty North  North Knoxville Medical Center  Peninsula Hospital  The Village  Parkwest Medical Center  Turkey Creek Medical Center  Blount Memorial Hospital  Methodist Medical Center  Ridgeview Psychiatric Hospital  Fort Loudon Medical Center  Le Conte Medical Center  Jefferson Memorial Hospital  St Mary's Med Ctr Campbell Cnty Featured Articles*Provider Directory Terms of Use: The WebMD 'Provider Directory' is provided by WebMD for use by the general public as a quick reference of information about Providers. The Provider Directory is not intended as a tool for verifying the credentials, qualifications, or abilities of any Provider contained therein. Inclusion in the Provider Directory does not imply recommendation or endorsement nor does omission in the Provider Directory imply WebMD disapproval. |
Suggested Reading on Genetic Counseling by Our Doctors
-
Related Diseases & Conditions
45 articles-
Colon Cancer
- Colon cancer is a malignancy that arises from the inner lining of the colon. Most, if not all, of these cancers develop from colonic polyps. Removal of
-
Breast Cancer
- Breast cancer is the most common cancer in women and the second most common cause of cancer death in women in the U.S. Symptoms include a lump in the breast
-
Miscarriage
- A miscarriage is any pregnancy that ends spontaneously before the fetus can survive. Miscarriage usually occurs before the 13th week of pregnancy. The
-
Down Syndrome
- Down syndrome is a chromosomal disorder that results in the presence of an additional third chromosome 21, also referred to as trisomy 21. Most individuals
-
Huntington's Disease
- Huntington's disease is the result of degeneration of neurons in areas of the brain. Huntington's disease is an inherited disorder. Early symptoms include
-
Marfan Syndrome
- Marfan syndrome is hereditary condition affecting connective tissue. A person with Marfan syndrome may exhibit the following symptoms and characteristics:
-
Ehlers-Danlos Syndrome
- Ehlers-Danlos syndromes are genetic disorders that include symptoms such as loose joints, tissue weakness, easy bruising, and skin that stretches easily.
-
Pheochromocytoma
- Pheochromocytoma is a tumor of the adrenal gland. Pheochromocytomas are quite rare and the vast majority of them are entirely benign. Only very rarely
-
Wolff-Parkinson-White Syndrome
- Wolff-Parkinson-White syndrome is a condition in which abnormal electrical pathways in the heart cause arrhythmias. Symptoms of Wolff-Parkinson-White syndrome
-
Phenylketonuria
- Phenylketonuria (PKU) is a disorder that is inherited. PKU disorder increases the levels of phenylalanine in the blood. Phenylalanine is an amino acid
-
Sickle Cell Disease (Sickle Cell Anemia)
- Sickle cell anemia (sickle cell disease), a blood disease which shortens life expectancy, is cause by an inherited abnormal hemoglobin. Symptoms may include
-
Beta Thalassemia
- Beta Thalassemia is the most familiar type of thalassemia. Thalassemia is not just one disease but rather a complex series of genetic (inherited) disorders
-
Amyotrophic Lateral Sclerosis (ALS)
- Amyotrophic lateral sclerosis (ALS, Lou Gehrig's disease) is a neurological disease that progresses rapidly. The disease attacks the nerve cells responsible
-
Ramsay Hunt Syndrome
- Ramsay Hunt syndrome is an infection of a facial nerve that causes a red painful rash with blisters and facial paralysis. The herpes zoster virus causes
-
Cerebral Palsy
- Cerebral palsy (CP) is an abnormality of motor function and postural tone acquired at an early age (even before birth). Cerebral palsy is generally caused
-
Angelman Syndrome
- Angelman syndrome is a genetic disorder that results from the absence of a functional copy of the UBE3A gene inherited from the mother. Infants with Angelman
-
Genetic Disease
- Genetic disease is a disorder or condition caused by abnormalities in a person's genome. Types of genetic inheritance include single inheritance (for example,
-
Fragile X Syndrome
- Fragile X syndrome is the most common inherited form of mental retardation. It's caused by a mutation on the X chromosome. People with Fragile X syndrome
-
Birth Defects
- Birth defects have many causes and currently, are the leading cause of death for infants in the first year of life. Some of the causes of birth defects
-
Achondroplasia
- A common form of short stature, achondroplasia (dwarfism) is a genetic condition causing a disorder of bone growth. Complications of achondroplasia that
-
Alpha Thalassemia
- Alpha thalassemia is a disorder in which the alpha globin protein is underproduced. There are two pairs of genes that carry the code for the alpha chains
-
Prader-Willi Syndrome
- Prader-Willi syndrome is a condition characterized by severe floppiness (hypotonia), poor growth, delayed development, and poor feeding problems in early
-
Gilbert Syndrome
- Gilbert syndrome is a benign genetic condition that causes abnormal breakdown of bilirubin, a compound that is formed when hemoglobin from red blood cells
-
Fabry Disease
- Fabry disease (Fabry's disease, alpha-galactosidase-A) is a genetic disorder with symptoms such as burning sensations in the hands, small-raised reddish-purplish
-
Alpha-1 Antitrypsin Deficiency
- Alpha-1 antitrypsin deficiency is an inherited disorder that may cause liver and lung disease in adults. Signs and symptoms include shortness of breath,
-
MELAS Syndrome
- MELAS syndrome, a rare form of dementia, stands for Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes. Mutations in the genetic material
-
Charcot-Marie-Tooth-Disease
- Charcot-Marie-Tooth disease is one of the most common inherited neurological disorders. Charcot-Marie-Tooth disease affects the peripheral nerves. Symptoms
-
Loeys-Dietz Syndrome
- Loeys-Dietz syndrome is a syndrome is an inherited genetic syndrome characterized by aortic aneurysms in children. Children with Loeys-Dietz syndrome are
-
Pick Disease
- Frontotemporal dementia (FTD) is a syndrome that is associated with shrinking of the frontal and temporal lobes of the brain. Frontotemporal dementia used
- See All Related Diseases & Conditions »
-
Colon Cancer
-
Medications
0 articles -
Procedures & Tests
4 articles -
Pictures, Images & Quizzes
0 articles -
Doctor's & Expert's Views
3 articles -
Health News
17 articles -
Health Features
0 articles
Women's Health Newsletter
Sign up to stay informed with the latest women's health-related updates on MedicineNet delivered to your inbox FREE!
BONUS! Get a Free PDF Women's Health Report when you sign up!
