Sanfilippo syndrome
Sanfilippo Syndrome (MPS III) | |
---|---|
Other names | Autism spectrum disorder[2] |
Prognosis | Lifespan is reduced; survival into adolescence or early adulthood |
Frequency | 1 in 70,000[3] |
Sanfilippo syndrome, also known as
Affected children generally do not show any signs or symptoms at birth, although some early indicators can be respiratory issues at birth, large head size, and umbilical hernia.[4] In early childhood, they begin to exhibit signs of developmental disability and loss of previously learned skills. In later stages of the disorder, they may develop seizures and movement disorders. Patients with Sanfilippo syndrome usually live into adolescence or early adulthood.[5]
Signs and symptoms
The disease manifests in young children, with symptoms usually beginning to appear between two and six years of age.
The disease progresses to increasing behavioral disturbances, including
In the final phase of the illness, children become increasingly
Individuals with MPS type III tend to have mild skeletal anomalies;
It is difficult to clinically distinguish differences among the four types of Sanfilippo syndrome. However, type A is usually the most severe subtype, characterized by its early onset, rapid clinical progression (with severe symptoms), and short survival rate.[12] The median age of death for children afflicted with type A is 15.4 ± 4.1 years.[13]
It is important that simple and treatable conditions, such as
Genetics
Mutations in four different genes can lead to Sanfilippo syndrome. This disorder is inherited in an
Sanfilippo syndrome type | Gene | Enzyme | Chromosomal region | Number of known mutations causing this type |
---|---|---|---|---|
Type A | SGSH | heparan N-sulfatase[14] |
17q25.3 | 137[citation needed] |
Type B | NAGLU | Alpha-N-acetylglucosaminidase[14] |
17q21.2 | 152[citation needed] |
Type C | HGSNAT | acetyl-CoA:alpha-glucosaminide N-acetyltransferase[14] |
8p11.21 | 64[citation needed] |
Type D | GNS | N-acetylglucosamine-6-sulfatase[14] | 12q14.3 | 23[citation needed] |
Mechanism
Glycosaminoglycans (GAGs) are
Diagnosis
Sanfilippo syndrome types A, B, C, and D are considered to be clinically indistinguishable, although mutations in different genes are responsible for each disease. The following discussion is therefore applicable to all four conditions.[citation needed]
A
The diagnosis may be confirmed by
Treatments
Treatment remains largely supportive. The behavioral disturbances of MPS-III respond poorly to medication. If an early diagnosis is made,
Several promising therapies are in development. Allievex was conducting a phase II/III clinical trial on Enzyme Replacement Therapy for MPSIIIB (former Biomarin clinical trail),[16][17] but negotiations to buy Allievex failed in December 2023, and the company abruptly terminated trials that had been reported to greatly improve child patients' condition as it could not raise enough money to support a new trial. This has been attributed largely to the economic difficulties in producing drugs for rare diseases, estimated to cost about five times more than treatments for common conditions.[18]
Ultragenyx (former Abeona clinical trial) and Lysogene of a gene therapy-based treatment for MPSIIIA.[19][20] Other potential therapies include chemical modification of deficient enzymes to allow them to penetrate the blood–brain barrier, stabilisation of abnormal but active enzyme to prevent its degradation, and implantation of stem cells strongly expressing the missing enzyme. For any future treatment to be successful, it must be administered as early as possible. Currently[when?] MPS-III is mainly diagnosed clinically, by which stage it is probably too late for any treatment to be very effective. Neonatal screening programs would provide the earliest possible diagnosis.[citation needed] The flavonoid genistein decreases the accumulation of GAGs.[21] In vitro, animal studies and clinical experiments suggest that the symptoms of the disease may be alleviated by an adequate dose of genistein.[22] Despite its reported beneficial properties, genistein also has toxic side effects.[23]
Several support and research groups have been established to speed the development of new treatments for Sanfilippo syndrome.[24][25][26][27] [28][excessive citations]
Participants in the first-ever "Caregiver Preference Study for Sanfilippo Syndrome" advocated for clinical trials that shift focus from primary cognitive outcomes to other multisystem endpoints, and perceptions of non-curative therapies revealed a preference for treatment options that stop or slow the disorder progression to maintain the child’s current function to ensure quality of life; thus, parents express high risk tolerance and a desire for broader inclusion criteria for trials.[29]
Prognosis
According to a study of patients with Sanfilippo syndrome, the median life expectancy varies depending on the subtype. In Sanfilippo syndrome type A, the mean age at death (± standard deviation) was 15.22 ± 4.22 years. For type B, it was 18.91 ± 7.33 years, and for type C it was 23.43 ± 9.47 years. The mean life expectancy for type A has increased since the 1970s.[30]
Epidemiology
Incidence of Sanfilippo syndrome varies geographically, with approximately 1 case per 280,000 live births in Northern Ireland,[31] 1 per 66,000 in Australia,[32] and 1 per 50,000 in the Netherlands.[33]
The Australian study estimated the following incidence for each subtype of Sanfilippo syndrome:
Sanfilippo syndrome type | Approximate incidence | Percentage of cases | Age of onset |
---|---|---|---|
A | 1 in 100,000[32] | 60% | 1.5–4 |
B | 1 in 200,000[32] | 30% | 1–4 |
C | 1 in 1,500,000[32] | 4% | 3–7 |
D | 1 in 1,000,000[32] | 6% | 2–6 |
Clinical care guidelines
The first-ever global consensus clinical care guidelines for Sanfilippo syndrome were published in Orphanet Journal of Rare Diseases[34] in late 2022. It represents a consensus set of basic clinical care guidelines that are accessible to clinicians and families globally. The guidelines consist of evidence-based, expert-led recommendations for how to approach Sanfilippo syndrome-specific care management and monitoring of disease-related changes. These clinical care guidelines are intended for use by anyone providing medical care, rehabilitative care, or support services for individuals with Sanfilippo syndrome. Additionally, the guidelines are a practical resource for families to be well-informed advocates and for them to share with their local care team, who may not have previous experience with this rare disease.
History
The condition is named after
Caregiver impact
Caregivers for children with Sanfilippo syndrome face a unique set of challenges because of the disease's complex nature. There is little understanding among clinicians of the family experience of caring for patients with Sanfilippo and how a caregiver's experiences change and evolve as patients age. The burden and impact on caregivers' quality of life is poorly defined and best-practice guidance for clinicians is lacking.[36]
A best-practice guidance to help clinicians understand the challenges caregivers face was published July 2019 in the Orphanet Journal of Rare Diseases by a group of international clinical advisors with expertise in the care of pediatric patients with Sanfilippo, lysosomal storage disorders, and life as a caregiver to a child with Sanfilippo.[36]
The group reviewed key aspects of caregiver burden associated with Sanfilippo B by identifying and quantifying the nature and impact of the disease on patients and caregivers. Recommendations were based on findings from qualitative and quantitative research.[36]
The article's authors reported, "Providing care for patients with Sanfilippo B impinges on all aspects of family life, evolving as the patient ages and the disease progresses. Important factors contributing toward caregiver burden include sleep disturbances, impulsive and hyperactive behavior, and communication difficulties ... Caregiver burden remained high throughout the life of the patient and, coupled with the physical burden of daily care, had a cumulative impact that generated significant psychological stress."[36]
Additionally, the authors call for changing the narrative associated with Sanfilippo: "The panel agreed that the perceived aggressive behavior of the child may be better described as 'physical impulsiveness' and is often misunderstood by the general public. Importantly, the lack of intentionality of the child’s behavior is recognized and shared by parents and panel members ... Parents may seek to protect their child from public scrutiny and avoid situations that may engender criticism of their parenting skills."[36]
Society and culture
The community of Sanfilippo families, foundations, scientists and researchers, and industry partners and collaborators around the world have dedicated November 16 as World Sanfilippo Awareness Day.[37][38]
World Sanfilippo Awareness Day is about spreading awareness and sparking conversations globally about Sanfilippo syndrome. This day of awareness is in honor of the children around the world living with Sanfilippo syndrome today, and those who have died. It also honors the families of the children with Sanfilippo syndrome. November 16, 2019, was the first year observing World Sanfilippo Awareness Day.
See also
- Mucopolysaccharidosis
- Hurler syndrome (MPS I)
- Hunter syndrome (MPS II)
- Morquio syndrome (MPS IV)
- List of neurological conditions and disorders
References
- ^ "Testing for Sanfilippo Syndrome". Cure Sanfilippo Foundation - Testing For Sanfilippo Syndrome. Cure Sanfilippo Foundation.
- ^ Marta Figeiredo (20 March 2018). "Autism Symptoms May Be Indicative of Sanfilippo Syndrome, Data Review Finds".
- ^ "Mucopolysaccharidoses Fact Sheet". National Institute of Neurological Disorders and Stroke. 15 Nov 2017. Retrieved 25 May 2018.
- ^ "Early Symptoms of Sanfilippo Syndrome". Cure Sanfilippo Foundation.
- ^ "Mucopolysaccharidosis type III". Genetics Home Reference. March 2017. Retrieved 22 July 2018.
- ^ a b c "A Guide to Understanding MPS III" (PDF). Archived from the original (PDF) on 8 July 2011. Retrieved 13 March 2019.
- PMID 20852935.
- PMID 29631636.)
{{cite journal}}
: CS1 maint: multiple names: authors list (link - PMID 29061114.)
{{cite journal}}
: CS1 maint: multiple names: authors list (link - S2CID 232273506.
- PMID 31536183. Retrieved 3 January 2023.
- ^ S2CID 24663642.
- PMID 24524415.
- ^ a b c d e f Edens Hurst, Anna C.; Zieve, David; Conaway, Brenda (1 May 2017). "Mucopolysaccharidosis type III". United States National Library of Medicine. Retrieved 20 June 2019.
- ^ a b Defendi, Germaine L. (23 May 2018). "Sanfilippo Syndrome (Mucopolysaccharidosis Type III)". Medscape. Retrieved 20 June 2019.
- ^ "Tralesinidase alfa for Sanfilippo syndrome type B". Allievex. Archived from the original on 2 June 2023. Retrieved 27 December 2023.
- S2CID 253759977.
- ^ Halliday, Josh (27 December 2023). "Sheffield family plead for help after drug trial for boy, 11, is abruptly stopped". The Guardian.
Tom Mathers, the chief executive of Allievex, said: "The hardest decision that I have ever had to make was to pause our ongoing treatment of children with this devastating disease. It is most frustrating because we have a treatment that we know works.
- ^ Koberstein, Wayne (November 7, 2018). "Lysogene: Mother of Invention". Life Science Leader. United States: VertMarkets.
- ^ Intracerebral Gene Therapy for Sanfilippo Type A Syndrome on clinicaltrials.gov
- ^ "Department of Molecular Biology, University of Gdansk - Head of DMB". Archived from the original on 2013-06-21. Retrieved 2014-01-07.
- PMID 16670689.
- PMID 17245525.
- ^ Cure Sanfilippo Foundation, funding research to accelerate discovery of a cure to Sanfilippo Syndrome
- ^ "Jonah's Just Begun - Foundation to Cure Sanfilippo, Inc". Archived from the original on 2021-06-19. Retrieved 2012-07-28.
- ^ Phoenix Nest, Inc., a biotech company seeking treatments and cures for Sanfilippo Syndrome
- ^ Phunk Phenomenon HipHop For Hope Archived 2018-09-01 at the Wayback Machine, a dance crew in Boston raising awareness for Sanfilippo Syndrome
- ^ Team Sanfilippo Foundation, a medical research foundation created by parents of children with Sanfilippo Syndrome
- PMID 33263924.
- PMID 29061114.
- S2CID 23099247.
- ^ S2CID 14297661.
- PMID 10480370.
- PMID 36303195.
- ^ Sanfilippo, S. J.; Podosin, R.; Langer, L. O., Jr.; Good, R. A. : Mental retardation associated with acid mucopolysacchariduria (heparitin sulfate type). J. Pediat. 63: 837-838, 1963.
- ^ PMID 31287005. Material was copied from this source, which is available under a Creative Commons Attribution 4.0 International License.
- ^ [Awareness Days - International Calendar] https://www.awarenessdays.com/awareness-days-calendar/world-sanfilippo-awareness-day-2019/ Archived 2020-10-25 at the Wayback Machine
- ^ [World Sanfilippo Awareness Day] https://curesanfilippofoundation.org/worldsanfilippoawarenessday/
External links
- Media related to Sanfilippo syndrome at Wikimedia Commons