WebDr. John C. Christianson is an infectious disease specialist in Franklin, Wisconsin and is affiliated with multiple hospitals in the area, including Aurora St. Luke's Medical Center and Ascension ... WebMay 15, 2024 · Genetic screening has identified numerous variants of the endosomal solute carrier family 9 member A6 (SLC9A6)/(Na +,K +)/H + exchanger 6 (NHE6) gene that cause Christianson syndrome, a debilitating X-linked developmental disorder associated with a range of neurological, somatic, and behavioral symptoms.Many of these variants cause …
Christianson Syndrome - GeneReviews® - NCBI Bookshelf
WebAug 11, 2014 · Christianson syndrome is a genetic disease that is transmitted through the affected X chromosome. Males have only one chromosome, while females have two X chromosomes in each cell. WebJul 30, 2024 · Weber-Christian disease is a rare inflammatory disease that affects the body's fat tissues. The disorder appears on the skin as red or purple tender, raised lumps usually on the thighs and lower legs. Other … csm doss fort rucker
Dr. John Christianson, MD - Infectious Disease ... - Healthgrades
WebChristianson syndrome Description Christianson syndrome is a disorder that primarily affects the nervous system. This condition becomes apparent in infancy. Its … Christianson syndrome is a rare genetic disorder. It causes severe problems with your nervous system. People with this condition have trouble walking and speaking. They typically also have developmental delays or intellectual disabilities. People with Christianson syndrome often start showing symptoms of the … See more Christianson syndrome mostly affects men and people assigned male at birth (AMAB). The condition is an “X-linked genetic disorder.” This means it occurs because of a change (mutation) in X chromosomes. See more Women and people assigned female at birth (AFAB) have two X chromosomes, while men and people AMAB have one X chromosome and … See more Experts don’t know exactly how many people have Christianson syndrome. They do know it’s extremely rare. By some estimates, about 1 in 600 boys have an X-linked intellectual … See more WebAffected males diagnosed with CS typically present with the following core diagnostic features: nonverbal status, intellectual disability (ID), epilepsy, ataxia, postnatal microcephaly, and hyperkinesis. Seizures typically occur prior to the age of three. Secondary symptoms include behaviors associated with autism, Angelman syndrome features ... csmd pool