Leuconnect is een platform voor de patiëntengemeenschap en hun families die getroffen zijn door leukodystrofie.
Het verbindt patiënten met elkaar. Dit platform ter ondersteuning van klinisch onderzoek bevordert studies op het gebied van leukodystrofieën.



Megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Article reviewed by Prof. Raul Estevez

Megalencephalic leukoencephalopathy with subcortical cysts (MLC) is a member of the family of leukodystrophies. It is an extremely rare genetic disease. Its frequency is less than 1 per 1,000,000 births, but the disease is more common in certain populations with high consanguinity. It is an orphan disease, which means that there is currently no treatment.


Alexander disease

Alexander disease is a rare genetic disorder in the family of demyelinating leukodystrophies. Its prevalence across the world is not exactly known, but has been estimated at 1 in 2,700,000 in Japan. This neurological disease is most often diagnosed in early childhood, but juvenile and adult forms also exist. Symptoms include mental retardation, epilepsy, and muscle stiffness, and their progression leads to the patient's death. It is characterised by a degeneration of the white matter and the formation of Rosenthal fibres.


Learn about Pelizaeus-Merzbacher disease (PMD)

Article reviewed by Prof. Nicole Wolf

Pelizaeus-Merzbacher disease (PMD) is a rare genetic disorder in the family of leukodystrophies. Its frequency is 1 per 100,000 births. It is one of the hypomyelinating leukodystrophies, white matter diseases characterised by a permanent deficit of myelin in the brain.


Leukoencephalopathy with thalamus and brainstem involvement and high lactate (or LTBL)

Leukoencephalopathy with thalamus and brainstem involvement and high lactate (or LTBL) is an extremely rare genetic disorder in the family of leukodystrophies. Its prevalence is less than one in 1,000,000. It is one of the hypomyelinating leukodystrophies, those white matter pathologies characterised by a permanent deficit of myelin in the brain.


VWM disease What's behind CACH syndrome?

Article reviewed by Prof. Nicole Wolf

CACH syndrome stands for Childhood Ataxia with Central Nervous System Hypomyelination. Today, the name leukoencephalopathy with vanishing white matter (VWM) is preferred. It is a genetic disease of the leukodystrophy family and it is one of the most common leukodystrophies, with a prevalence of about 1 in 80,000. It is one of the hypomyelinating leukodystrophies secondary to astrocyte damage. VWM disease displays a progressive degradation of the white matter in the brain.


Krabbe disease or globoid cell leukodystrophy

Krabbe disease is a rare hereditary disease that affects the white matter of the central (brain and spinal cord) and peripheral (nerves of the lower and upper limbs) nervous systems.


Better understanding of Metachromatic Leukodystrophy

Metachromatic Leukodystrophy (MLD) is a member of the lysosomal leukodystrophy family. It's a rare autosomal recessive genetic disorder. Its frequency is 1 per 45,000 births. It can begin in childhood, adolescence or adulthood and leads to severe neurological dysfunction affecting motor and cognitive functions that can lead to death.



X-linked adrenoleukodystrophy (ALD) is a worldwide genetic disease, rare and serious, of the family of leukodystrophies. Its incidence of 1 for 17 000 births makes it, however, the most common type of leukodystrophy. It is a metabolic disease which affect the brain, the bone marrow and peripheral nerves, but also the adrenal (and the testis) as part of its name « adreno- » refers to.


Anticipatory Guidance in Aicardi Goutieres Syndrome (AGS)

From: Dr. Adeline Vanderver
Program Director of the Leucodystrophy Center of Excellence - Children’s Hospital of Philadelphia, Philadelphia, PA 19104 – USA

Aicardi Goutieres Syndrome (AGS) is a genetically heterogeneous disorder that can be caused by mutations in a series of genes with a final endpoint of upregulation of the IFN pathway and the innate immune system.


Bone marrow transplant and gene therapy as treatments for leukodystrophies

In this article we will first describe the procedures of bone marrow transplant and gene therapy, before describing the applications and results obtained in leukodystrophies.

Het nieuws


Een zesde taal voor Leuconnect

Het internationale succes van Leuconnect maakt het platform groeien.

Het Nederlands is nu toegevoegd aan de vijf talen die al worden aangeboden.

De klinische studies vermenigvuldigen zich op Leuconnect en de betrokken onderzoekers vertalen hun tevredenheid door het uitvoeren van hun studies op het platform te vernieuwen. Hun ervaringen, evenals die van families, voeden de evolutie van het instrument om beter in de behoeften te voorzien.

ELA International blijft zich inzetten voor het bieden van toegang tot online klinische studies aan zoveel mogelijk patiënten.

Vanaf nu is het platform toegankelijk voor patiënten in het Nederlands en onderzoekers die dit wensen kunnen ook hun studies in deze taal uitvoeren.


SMART-ALD - Neue Lifestyle-Intervention zur Verbesserung der Lebensqualität bei Frauen mit X-ALD

Was ist SMART-ALD?

Die SMART-ALD-Studie hat das Ziel, das körperliche und psychische Wohlbefinden und die Lebensqualität von symptomatischen Frauen mit X-ALD durch ein neues, multidisziplinäres Behandlungsangebot langfristig zu verbessern. Mit dieser klinischen Studie möchten wir die Machbarkeit, Akzeptanz und Wirksamkeit einer neuen Lifestyle-Intervention als ein intensiviertes Versorgungsprogramm für Frauen mit X-ALD unter Verwendung von Video-Sprechstunden prüfen.


Quality of life study of women with X-ALD on Leuconnect: 2 new sites

Launch of a study on the quality of life of women with X-ALD on Leuconnect

A study on the quality of life of women with X-linked adrenol-cholodystrophy opens in Spanish and Italian on Leuconnect. This study is an extension of a first version available in English, French and German. If you have not yet participated in this study and speak one of these two languages, you can apply for the study.


Study on ALDc patients and their caregivers - Results

To better understand the impact of Cerebral Adrenocleucodystrophy CALD) on the quality of life of patients and their families

Adrenoleukodystrophy (ALD) is a rare metabolic disorder caused by mutations in the ABCD1 gene that lead to a toxic accumulation of very long-chain fatty acids (VLCFAs). It is an X-linked disease that mainly affects boys. About 40% of them will develop the cerebral form of the disease (CALD). Early diagnosis of CALD is essential to enable treatment to be administered before symptoms appear and the disease progresses.


Study opened: Women with Adrenoleukodystrophy

Quality of life in women with X-ALD

X-linked Adrenoleukodystrophy (X-ALD) is a hereditary disease caused by mutations in the ABCD1 gene leading to disturbances in the metabolism of fatty acids. This results in an accumulation of very long chain fatty acids in the cells of the body causing damage to the central nervous system (white matter of the brain and spinal cord). The most common clinical form of X-ALD is adrenomyeloneuropathy (AMN), in which the symptoms usually first appear in early adulthood.


Assessing the impact of cerebral adrenoleukodystrophy (CALD) on patients and their families - Completed

There are no studies in France on the burden of cerebral adrenoleukodystrophy (CALD) on the children affected and their families.

In partnership with ELA International, and accompanied by ARGO Santé, a health research and consulting firm, BlubirdBio is launching a study on the impact of the disease on boys with CALD.


Opening of the Orchard-MLD study - Completed

Impact of MLD
Thank you for your interest in participating in the study entitled "Exploring the Burden of Disease and Quality of Life in people with Metachromatic Leukodystrophy (MLD) in the United States and Europe: A Descriptive Study".  This study is an international research programme that is being offered to the United States and some countries in Europe, including France. It is offered to parents of children with MLD or relatives of sick children to better understand the impact of the disease on patients and their families beyond the direct medical implications that it causes.


Practical guide to registering your telephone number

Your mobile phone number is required when you register on the Leuconnect platform.
It will allow you to receive your connection codes.

N.B.: Please make sure that you follow the format requested.


Laten we samen onderzoek versnellen. Registreer u op LEUCONNECT!

Aangezien leukodystrofieën zeldzame ziekten zijn, zijn er te weinig patiënten betrokken bij onderzoek naar deze ziekten, terwijl ze vaak een grote kennis van hun pathologie hebben verworven Hiervoor hebben ELA France en ELA International LEUCONNECT opgericht, een ondersteuningsplatform voor klinisch onderzoek.


Tutorial videos to better use Leuconnect

New things on Leuconnect !
With the support of Fondation Roche, ELA created tutorial videos to help you with your registration on the website and with its use. Four videos are provided to help you navigate the platform.


Leuconnect development

Leuconnect is a platform created at the initiative of ELA families to enable leukodystrophy patients and their parents to form a virtual, voluntary cohort to advance leukodystrophy research by participating in clinical studies.


Leuconnect om deel te nemen aan klinische onderzoeken.

U bent lid van het Leuconnect e-cohort, en zo krijgt u eenvoudig toegang tot klinische onderzoeken en kunt u een echte rol spelen in onderzoek.

Het versnellen van onderzoek op het gebied van leukodystrofieën is een van de grootste uitdagingen van de ELA-vereniging en de belangrijkste doelstelling van Leuconnect. Door de rekrutering van patiënten en hun toegang tot open klinische onderzoeken op het platform te vergemakkelijken, bevordert Leuconnect de uitvoering van klinische onderzoeken. De patiënten die zijn ingeschreven in het cohort vormen samen een gemeenschap, beschikbaar en gemotiveerd om deel te nemen aan online onderzoeken.


Communiceren dankzij LEUCONNECT

In het vorige nummer van uw tijdschrift ELA info heeft u kunnen lezen hoe u zich op LEUCONNECT kunt inschrijven en deelnemen aan het patiëntencohort. U bent lid van het LEUCONNECT-cohort, en u kunt eindelijk communiceren met andere families die getroffen zijn door leukodystrofieën. Samen vormt u een gemeenschap.
In dit nummer leest u hoe u op LEUCONNECT kunt communiceren.


Uw "patiëntendossier" op Leuconnect invullen

In eerdere uitgaven van het tijdschrift ELA Info heeft u gezien hoe u zich kunt inschrijven voor het Leuconnect-cohort en hoe u kunt communiceren met het beveiligde interne berichtensysteem.

Vandaag ontdekt u hoe u uw "patiëntendossier" kunt invullen. Het groepeert een verzameling gegevens over uw pathologie, de omstandigheden en de evolutie ervan.
Hiermee kunt u uw ziekte volgen.


Welcome on Leuconnect!

ELA France and ELA International are launching Leuconnect, an online platform dedicated to help clinical research by facilitating recruitment of patients into studies and clinical trials, to help the acceleration of research on leukodystrophies in France and worldwide.