expertise centrum Cornelia de Lange syndroom

welcome

at the expertise centrum Cornelia de Lange syndroom

Goal of expertise centrum Cornelia de Lange syndroom

Goal of the expertise centrum Cornelia de Lange syndroom

The Cornelia de Lange Syndrome expertise centre is there for all people with Cornelia de Lange syndrome and their families and/or carers. As a centre of expertise, we combine our knowledge of the syndrome and support and advise patients, their families and their treating physicians. 

Services/Qualifications expertise centrum Cornelia de Lange syndroom

Clinical centre
1Availability of a specialized multidisciplinary approach to patients in a specific for the decease clinic in a medical facility
2Evidence for a strong knowledge base of decease
3Commitment to furthering clinical knowledge of decease ideally in a collaborative way
4Dissemination of new clinical information of decease either via national and/or international meetings or publications
5Having received funding for decease-relevant specific areas
Research Centre
6Research which provides a significant contribution towards understanding the science behind the decease
7Evidence for a strong knowledge base of the decease
8Commitment to furthering scientific knowledge of the decease ideally in a collaborative way
9Having received funding for decease-relevant research
10Dissemination of new scientific findings related to decease via (inter)national meetings, publications or significant contributions
Practical information

Practical information

Make an appointment

The consultation hours of the expertise centre take place on every 2nd and 4th Tuesday afternoon of the month. If you would like to make an appointment for the consultation hour, please send an e-mail. You can send the referral letter from your doctor, for example the general practitioner or another specialist, with this e-mail. You can also indicate on which Tuesdays you could visit the outpatient clinic in the coming months. When planning your appointment, we will take your preferred day(s) into account as much as possible.

Bring along

We ask you to bring the following with you when visiting the clinic:
Appointment confirmation
Appointment confirmation.
AUMC patient card and appointment card, if you already have one.
AUMC patient card and appointment card, if you already have one.
Valid insurance card the person with Cornelia de Lange syndrome
Valid insurance card the person with Cornelia de Lange syndrome.
Identity card of the person with Cornelia de Lange syndrome and yourself
Identity card of the person with Cornelia de Lange syndrome and yourself (passport, driving licence, identity card or * tourist card).
Growth data
Growth data information of the consultation bureau, if available.
List of medication and specially adapted aids
List of medication and specially adapted aids, if applicable.
Familiar toys
Familiar toys for your child, if desired.
Brieven
Letters about your child written by other doctors, if you have them.
Costs

Costs

Visits to the expertise clinic are generally reimbursed by your health insurer (when you are a resident of The Netherlands). We ask you to contact your insurer prior to your appointment to ask whether your visit to an expertisepoli is indeed reimbursed. If this is not the case, we would like to ask you to mail us this prior to your appointment.
Contact

Contact

expertise centrum Cornelia de Lange syndroom
( Department of AMC Expertise centrum Cornelia de Lange )

Polikliniek Kindergeneeskunde, bouwdeel A0, wachtkamer 2
Meiwerfdreef 9
Postbus 22660
1100 DD Amsterdam
Nederland

phone: 020 566 8000

About the website contents

All of the information contained within these questions and answers is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know, contact see below.