Cheyenne And Tristan, Dealing with Joubert Syndrome: Chey the morning after 1st surgery

she was checking out her red finger she thought it was cool for a little while then just wanted it off

What is Joubert Syndrome?

Joubert syndrome is a rare brain malformation characterized by the absence or underdevelopment of the cerebellar vermis - an area of the brain that controls balance and coordination. The most common features of Joubert syndrome in infants include abnormally rapid breathing (hyperpnea), decreased muscle tone (hypotonia), jerky eye movements (oculomotor apraxia), mental retardation, and the inability to coordinate voluntary muscle movements (ataxia). Physical deformities may be present, such as extra fingers and toes (polydactyly), cleft lip or palate, and tongue abnormalities. Kidney and liver abnormalities can develop, and seizures may also occur.. Most cases of Joubert syndrome are sporadic (not inherited). In some families, however, Joubert syndrome appears to be inherited in an autosomal recessive manner (meaning both parents must have a copy of the mutation) via mutation in a number of genes, including NPHP1, AHI1, and CEP290.

Cheyenne And Tristan, Dealing with Joubert Syndrome

Cheyenne

Tristan

Friday, July 9, 2010

Chey the morning after 1st surgery

No comments:

Post a Comment

About Us

Blog Archive

Playing in the tent

Followers