Get the free Cornelia de Lange Syndrome Foundation Research Application

Este formulario de solicitud de investigación está diseñado para recopilar información relevante de los solicitantes que deseen recibir financiación para estudiar el Síndrome de Cornelia de

How to fill out cornelia de lange syndrome

How to fill out Cornelia de Lange Syndrome Foundation Research Application

1. Begin by visiting the Cornelia de Lange Syndrome Foundation's official website.
2. Navigate to the research application section of the site.
3. Download the application form and guidelines provided.
4. Carefully read the eligibility criteria and ensure your project aligns with their research priorities.
5. Fill out the application form, providing detailed information about your research project, objectives, and methodology.
6. Attach any necessary documentation, including research credentials and relevant past work.
7. Review your application for completeness and accuracy.
8. Submit the application by the specified deadline, using the preferred submission method outlined in the guidelines.

Who needs Cornelia de Lange Syndrome Foundation Research Application?

1. Researchers and scientists working on studies related to Cornelia de Lange Syndrome.
2. Academic institutions looking to fund or support research in this area.
3. Clinicians interested in developing better treatment strategies for patients with Cornelia de Lange Syndrome.
4. Organizations seeking to advance knowledge and understanding of the syndrome.

People Also Ask about

Is Cornelia de Lange syndrome a form of dwarfism?

The syndrome is named after Dutch pediatrician Cornelia Catharina de Lange, who described it in 1933. It is often termed Brachmann de Lange syndrome or Bushy syndrome and is also known as Amsterdam dwarfism. Its exact incidence is unknown, but it is estimated at 1 in 10,000 to 30,000.

What is the average lifespan of someone with Cornelia de Lange syndrome?

Life expectancy is somewhat normal for people with Cornelia de Lange syndrome. Most children with the condition live well into adulthood. But if your child has certain features of the disease, they may decrease life expectancy. These features include heart and throat defects.

What is Cornelia de Lange syndrome in English?

Cornelia de Lange syndrome (CdLS) is a rare genetic condition that affects growth and development and can range from mild to severe. A child's growth before and after birth is often slower, and they may have short stature.

What is the IQ of a person with Cornelia de Lange syndrome?

Most individuals with classic CdLS have been reported to have severe to profound intellectual disability with IQs ranging from 30 to 86 (mean 53). There is currently no cure for this disorder.

How rare is Cornelia de Lange syndrome?

Although the exact incidence is unknown, Cornelia de Lange syndrome likely affects 1 in 10,000 to 30,000 newborns. The condition is probably underdiagnosed because affected individuals with mild or uncommon features may never be recognized as having Cornelia de Lange syndrome.

What are the odds of getting Cornelia de Lange syndrome?

Although the exact incidence is unknown, Cornelia de Lange syndrome likely affects 1 in 10,000 to 30,000 newborns. The condition is probably underdiagnosed because affected individuals with mild or uncommon features may never be recognized as having Cornelia de Lange syndrome.

How long do people with Cornelia de Lange syndrome live?

A person with CdLS can live a normal lifespan.

What are the behaviors of a person with Cornelia de Lange syndrome?

Individuals with CdLS have autistic features characterized by repetitive behaviors, self-injurious behaviors, and deficits in communicative abilities, with less impact on social deficits. Common associated behavioral manifestations in individuals with CdLS include hyperactivity, anxiety symptoms, and sleep problems.

For pdfFiller’s FAQs

What is Cornelia de Lange Syndrome Foundation Research Application?

The Cornelia de Lange Syndrome Foundation Research Application is a formal proposal submitted by researchers seeking funding or support for studies and projects related to Cornelia de Lange Syndrome (CdLS), aimed at furthering understanding and treatment of the condition.

Who is required to file Cornelia de Lange Syndrome Foundation Research Application?

Researchers, scientists, or institutions conducting studies related to Cornelia de Lange Syndrome are required to file the Cornelia de Lange Syndrome Foundation Research Application when seeking funding or support from the foundation.

How to fill out Cornelia de Lange Syndrome Foundation Research Application?

To fill out the Cornelia de Lange Syndrome Foundation Research Application, researchers must complete the designated application form, providing detailed information about their project, including objectives, methodology, budget, timeline, and relevance to CdLS.

What is the purpose of Cornelia de Lange Syndrome Foundation Research Application?

The purpose of the Cornelia de Lange Syndrome Foundation Research Application is to evaluate and support scientific research initiatives aimed at understanding, diagnosing, and treating Cornelia de Lange Syndrome, ultimately enhancing the quality of life for affected individuals.

What information must be reported on Cornelia de Lange Syndrome Foundation Research Application?

The application must report information such as the research title, objectives, background and significance, research design and methods, expected outcomes, project timeline, budget details, and the credentials of the research team.