Aicardi syndrome is a rare genetic condition that affects 300-500 people worldwide, nearly all of them females. Symptoms of Aicardi syndrome usually first become apparent between three and five months ...

Aicardi syndrome is a rare genetic condition that mainly affects newborn females. The condition is characterized by a partial or complete absence of an important brain structure called the corpus ...

Aicardi-Goutières syndrome is a rare progressive encephalopathy characterized by a typical clinical picture, bilateral basal ganglia calcifications, leukodystrophy and brain atrophy ...

The Aicardi Goutieres Syndrome market growth is driven by factors like increase in the prevalence of Aicardi Goutieres Syndrome, investments in research and development, entry of emerging ...

LOS ANGELES — Introduction of a ketogenic diet reduced seizure burden in children with Aicardi syndrome as soon as 3 months, with beneficial long-term effects, according to a poster at the ...

Nikki Moberly's daughter, Erin, pictured, was diagnosed with Aicardi Syndrome as a young girl. Nikki Moberly Erin was eligible for early intervention services allowing her to go to school at age ...

4-year-old "Bobbi" Dougharty was born with a rare genetic disorder called Aicardi Syndrome, because of this she goes through life in a wheelchair.

Caitlin was born with a very rare neurodevelopmental disorder called Aicardi syndrome and requires 12 different specialists who care for her at Lurie.

The Aicardi Syndrome Foundation estimates there are only 1,000 cases in the U.S. and roughly 4,000 worldwide. Brooke has experienced medical hardship her whole life.

Severe pyramidal syndrome with tetraparesis left > right, spasticity, marked tendon hyperreflexia, positive Babinski reflexes bilaterally, dysphagia, trunk hypotonia, absent head and neck control ...