First clinical guideline on Schaaf-Yang syndrome for professionals and families


The research team reviewed all the articles and studies on Schaaf-Yang syndrome that had been published, with the aim of producing a comprehensive clinical guideline for healthcare professionals and families.

The research team reviewed all the articles and studies on Schaaf-Yang syndrome that had been published, with the aim of producing a comprehensive clinical guideline for healthcare professionals and families.


Guia genètica

Guia genètica

Improving knowledge of the Schaaf-Yang syndrome (SYS) -an ultrarare disease caused by mutations in the MAGEL2 gene- is the aim of the first clinical guideline aimed at healthcare professionals and families of children affected by this pathology. The article, published in the Journal of Medical Genetics, has revealed the effects of the truncated MAGEL2 protein on cell physiology.

The article is based on a project led by researchers Raquel Rabionet and Susanna Balcells, from the Faculty of Biology and the Institute of Biomedicine (IBUB) of the University of Barcelona, the Sant Joan de Déu Research Institute (IRSJD) and the Rare Diseases Networking Biomedical Centre (CIBERER), and Roser Urreizti, CIBERER researcher attached to the Sant Joan de Déu Research Institute and the Hospital Sant Joan de Déu Barcelona, with the participation of research teams from the aforementioned institutions.

Schaaf-Yang syndrome (SYS) is an ultrarare disease caused by mutations in the MAGEL2 gene, located on chromosome 15. The MAGEL2 gene is mainly expressed in the brain and its protein is key in the transport complex and the recycling regulation of certain proteins within cells. Patients with SYS show a wide variety of clinical signs and symptoms, the most common of which are neurodevelopmental and intellectual delay, sleep disturbance, facial dysmorphism and joint contractures.

The involvement of families and associations is key in the search for rare diseases

The loneliness of having an ultrarare disease is one of the great difficulties faced by affected families. Currently, only 11 cases of Schaaf-Yang syndrome are known in Spain, and less than 200 worldwide. This low incidence makes standardised medical care difficult, as there are neither clear clinical guidelines nor specific or follow-up treatments.

“Often, families and professionals face a great uncertainty due to a lack of information. For this reason, it is vital to have evidence-based recommendations that help improve clinical care and empower families about the natural course of the disease”, notes Merche Serrano, neuropaediatrician at the Sant Joan de Déu Barcelona Hospital, researcher at the IRSJD and coordinator of the clinical part of the study.

An evidence-based guide for professionals and families

The research team reviewed all the articles and studies on SYS that had been published, with the aim of producing a comprehensive clinical guideline for healthcare professionals and families, so that both groups would have more knowledge about the disease when taking care of the patients.

The clinical guideline includes the most relevant medical problems divided into two time periods: the first includes the first 28 days of life, and the second includes childhood and adolescence. The most appropriate interventions for each problem have also been indicated, as well as the best possible follow-up guidelines. This guide aims to ensure the best possible care for all children.

“We have also made a guideline and material aimed at families, at the request of the Schaaf-Yang Syndrome Families Association, which will help them learn about the evolution of the disease and will empower them”, says Roser Urreizti. “For us, it is very important to work closely with families and patients, especially in minority diseases where patients play a key role in advancing in the research”, concludes the researcher.

The toxic effect of the truncated protein MAGEL2

The extensive review of the scientific literature has also mapped all the mutations in the MAGEL2 gene, most of which result in a truncated (non-functional) protein or a protein with a partial or complete lack of the MHD domain, leading to a malfunctioning of the protein.

The MAGEL2 gene is located on chromosome 15 and it produces the MAGEL2 protein, which is part of the endosomal protein recycling and retrograde transport complex, as well as other functions.

“Our studies show that the mutated MAGEL2 protein is retained in the nucleus of cells, where it may alter the expression and regulation of other genes, while exerting a toxic effect on the cell. We observed low levels of beta-amyloid (Aß) 1-40 and intracellular glutamine in fibroblasts from the patients. These two molecules could serve as possible biomarkers to evaluate future treatments”, says Laura Castilla, first author of the study (UB-IBUB-IRSJD-CIBERER).

The results confirm that the phenotype of Schaaf-Yang syndrome could cause this toxic effect of the truncated MAGEL2 protein, rather than the lack of normal functionality as observed in fibroblasts from the patients the researchers studied.

The predoctoral researchers Mònica Centeno and Aina Prat will continue these studies with the analysis of MAGEL2 function in brain organoids generated from patient-derived pluripotent cells.

Reference article:

Castilla-Vallmanya, L.; Centeno-Pla, M.; Serrano, M. et al. «Advancing in Schaaf-Yang syndrome pathophysiology: from bedside to subcellular analyses of truncated MAGEL2». Journal of Medical Genetics, September 2022. Doi:10.1136/ jmedgenet-2022-108690

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