Familial HypopituitarismSymptoms, Doctors, Treatments, Advances & More
Learn About Familial Hypopituitarism
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However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.
Avera Medical Group Internal Medicine — 69th & Louise
Stuart Andersen, MD, provides internal medicine services at Avera Medical Group Internal Medicine in Sioux Falls, SD. Dr. Andersen is rated as an Advanced provider by MediFind in the treatment of Familial Hypopituitarism. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Familial Hypopituitarism, Sepsis, Pneumonia, Endoscopy, and Pacemaker Implantation. Dr. Andersen is board certified in American Board Of Internal Medicine, Internal Medicine.
Louise Gregory practices practicing medicine in London, United Kingdom. Ms. Gregory is rated as an Elite expert by MediFind in the treatment of Familial Hypopituitarism. She is also highly rated in 22 other conditions, according to our data. Her clinical expertise encompasses Familial Hypopituitarism, Hypopituitarism, Septo-Optic Dysplasia, and Cardiofaciocutaneous Syndrome.
Mohamad Maghnie practices practicing medicine in Genoa, Italy. Mr. Maghnie is rated as an Elite expert by MediFind in the treatment of Familial Hypopituitarism. He is also highly rated in 37 other conditions, according to our data. His clinical expertise encompasses Familial Hypopituitarism, Hypopituitarism, Neurohypophyseal Diabetes Insipidus, Pediatric Growth Hormone Deficiency, and Hormone Replacement Therapy (HRT).
Summary: Our vision, that of the researchers at the University of Texas Health Science Center at San Antonio, is that every person with a chromosome 18 abnormality will have an autonomous and healthy life. Our mission is to provide families affected by chromosome 18 abnormalities with comprehensive medical and educational information. Our goals are to provide definitive medical and education resources for ...
Summary: Turner syndrome (TS) is a rare chromosomal disorder characterized by partial or complete loss of one of the X chromosomes that affects about one in every 2000 female babies born. These young patients described difficulties making friends, understanding others' emotions and intentions, and controlling their own emotions. Difficulties in these domains could led to social withdrawal, to reduced socia...