How long can a person with Wolf-Hirschhorn syndrome live?

How long can a person with Wolf-Hirschhorn syndrome live?

The median survival time for de novo deletions was 34+ years while for translocation cases it was 18+ years. CONCLUSIONS—The mortality rate is lower than previously reported. There is a statistically significant relationship between deletion size and overall risk of death in de novo deletion cases.

Can people with Wolf-Hirschhorn syndrome talk?

Although most children with this syndrome are severely limited in communicative abilities, the school-based speech-language pathologist working with a special education caseload may encounter WHS children with smaller deletions (and thus less severe phenotypes) who may profit from speech language pathology services.

What is the wolf syndrome?

Wolf-Hirschhorn syndrome is a condition that affects many parts of the body. The major features of this disorder include a characteristic facial appearance, delayed growth and development, intellectual disability, and seizures.

Can a person with Wolf-Hirschhorn syndrome have children?

A loss of these genes results in the intellectual disability , slow growth, and other health problems characteristic of Wolf-Hirschhorn syndrome. If a parent is found to have a balanced translocation involving chromosome 4, they may be at risk of having additional children with Wolf-Hirschhorn syndrome.

Can you prevent Wolf-Hirschhorn syndrome?

There is no cure for Wolf-Hirschhorn syndrome, and every patient is unique, so treatment plans are tailored to manage the symptoms.

How is Miller syndrome treated?

Treatment for Miller Fisher syndrome is identical to treatment for Guillain-Barré syndrome: intravenous immunoglobulin (IVIg) or plasmapheresis (a procedure in which antibodies are removed from the blood) and supportive care. The prognosis for most individuals with Miller Fisher syndrome is good.

How old is the oldest person with lissencephaly?

The oldest known person to have lived with lissencephaly died at age 30. To care for Carter full time, Mary Pederson quit her job as an educational support professional at the William Pittaway School, where she worked with children with autism.