What is Maroteaux-Lamy
April 28, 2008 by planetultramarathon
http://www.mpssociety.co.uk/maroteaux.htm
Maroteaux-Lamy Disease (MPS VI)
Maroteaux-Lamy disease, also known as MPS VI, is one of the rarer mucopolysaccharide diseases. It takes its name from two French doctors, Dr Maroteaux and Dr Lamy, who first described the condition in 1963.
The disease varies enormously in the severity of the problems it causes. It is important to remember this variation if you are a parent of a newly diagnosed child. There are a range of possible symptoms but this does not mean your child will experience them all, or that he or she will be severely affected by them. In fact some patients have very few physical problems and are able to lead a relatively normal life.
What causes Maroteaux-Lamy disease?
There is a continuous process in the body of replacing used materials and breaking them down for disposal. Children with Maroteaux-Lamy disease are missing an enzyme which is essential in cutting up the mucopolysaccharide called dermatan sulphate. The incompletely broken down mucopolysaccharides cannot be used in the proper development of bones and cartilage and remain stored in cells in the body causing progressive damage. Babies may show little sign of the disease but, as more and more cells become damaged, symptoms start to appear.
How common is Maroteaux-Lamy disease?
The MPS Society has data which show that over a ten-year period 5 babies with Maroteaux-Lamy disease were born in Britain. A particularly severe form of the disease has been reported among Australian aborigines. It also occurs in Siamese cats.
How is the disease inherited?
We all have genes inherited from our parents which control whether we are tall, short, fair etc. Some genes we inherit are ‘recessive’, that is to say we carry the gene but it does not have any effect on our development. Maroteaux-Lamy disease is caused by a recessive gene. If an adult carrying the abnormal gene has a partner who is another carrier there will be a one in four chance with every pregnancy that the child will inherit the defective gene from each parent and will suffer from the disease. There is a two in three chance that unaffected brothers and sisters of children with Maroteaux-Lamy disease will be carriers. They can be reassured however that, as the disease is so rare, the chance of having a partner who is another carrier is very slight as long as their partner is not a cousin or other blood relative.
All families of affected children should seek further information from their doctor or genetic counsellor before planning to have more children. There is a more detailed explanation of this complex subject in the booklet on the pattern of inheritance available from the MPS Society.
At the time of writing there are no tests which can predict whether a child will be mildly or severely affected.
Is there a cure?
Bone marrow transplants have been used to treat patients with Maroteaux-Lamy disease and, although not a cure, have helped to relieve some of the symptoms of the disease. There are considerable risks involved in bone marrow transplantation and it is important to take time to weigh up these risks and the possible advantages. If you wish, the Society can put you in touch with parents whose children have already had this treatment so that you can be better informed before taking a decision.
It is possible that one day a laboratory may be able to produce the missing enzyme which could then be given to patients to replace what they are lacking (enzyme replacement therapy). Progress is being made but it is important to recognise that research programmes take many years and are often affected by unexpected delays. At the time of writing no one can say when or if such a treatment will be available.
Prenatal diagnosis
If you already have a child with Maroteaux-Lamy disease, it will be possible to have tests during a subsequent pregnancy to find out whether the baby you are carrying is affected. It is important to contact your doctor as soon as you suspect that you may be pregnant if you wish tests to be arranged. If you have any difficulty please contact the Society without delay.
http://www.emedicine.com/PED/topic1373.htm
Background
The mucopolysaccharidoses (MPS) are a group of inherited disorders that result from the deficiency of 1 or more of the lysosomal enzymes required for glycosaminoglycan (GAG) catabolism. GAGs, which are a major constituent of connective tissues, are long-chain complex carbohydrates that are usually linked to proteins to form proteoglycans and include chondroitin 4-sulfate, chondroitin 6-sulfate, heparan sulfate, dermatan sulfate, keratan sulfate, and hyaluronic acid. Because GAGs are primarily found in connective tissue, the sites of pathology primarily include the skeleton, heart valves, and other areas with connective tissue stroma.
The clinical features of the MPS result from lysosomal accumulation of partially degraded or undegraded GAGs and typically include coarse facies, corneal clouding, organomegaly, joint stiffness, dysostosis multiplex, hernias, short stature, and, in some disorders, mental retardation. The specific enzymatic deficiency and the resultant pattern of GAG degradation products determine the phenotype of each disorder. In general, dermatan, keratan, and chondroitin sulfate degradation products are associated with visceral manifestations, whereas the accumulation of heparan sulfate degradation products may be associated with mental deficiency. MPS VI, which is inherited as an autosomal recessive trait, results from the deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B) activity and the lysosomal accumulation of dermatan sulfate. MPS VI is characterized by somatic features but not by mental retardation.
Pathophysiology
MPS VI is characterized by progressive connective-tissue organ involvement that results from continuous storage of dermatan sulfate in the skeleton, heart valves, spleen, liver, and cornea. Pathological examination of affected tissues reveals the presence of engorged lysosomes. Patients appear healthy at birth and have accelerated growth in the first year, followed by deceleration and short stature later in childhood. The diagnosis is usually made in early childhood when organomegaly, corneal clouding, coarse features, enlarged tongue, and joint stiffness are all apparent. Other complications include hearing loss, chronic respiratory tract infections, sleep apnea, pulmonary hypertension, hydrocephalus, rapid-onset blindness, and cardiac valve insufficiency or stenosis.
Frequency
United States
The MPS are rare disorders, and data concerning incidence are not widely available.
International
Several reports provide estimates of MPS VI incidence outside the United States. An Australian survey reported an incidence rate of 1 per 248,000 births from 1980-1996 (Nelson, 2003). Recent reports from Germany, the Netherlands, and northern Portugal noted birth incidences of 1 per 434,783, 1 per 667,000, and 1 per 238,095, respectively (Baehner, 2005; Poorthuis, 1999; Pinto, 2004).
Mortality/Morbidity
MPS VI is characterized by substantial morbidity because of progressive accumulation of GAGs.
- Although mental development is normal, physical and visual defects can adversely affect psychomotor development.
- Growth may be normal for the first few years of life but then stops, resulting in dwarfism.
- Most patients have corneal clouding, which can interfere with vision.
- Restricted joint movement is a common feature, and patients develop claw-hand deformities due to contractures.
- Cardiac involvement includes aortic and mitral valve dysfunction.
- Skeletal changes are typified by dysostosis multiplex.
- Patients may also have obstructive airway disease.
- Age at death is variable, and mild forms of the disease have been described with prolonged survival.
Race
MPS VI is panethnic.
Sex
MPS VI is inherited as an autosomal recessive trait and appears equally in males and females.
Age
MPS VI is an inherited disorder that typically manifests in early childhood with retarded growth, hepatosplenomegaly, and coarse facial features.
History
- Affected individuals usually have a period of normal growth and development but later present when hepatosplenomegaly, coarse facial features, joint or spine abnormalities, and corneal clouding become evident.
- Because mucopolysaccharidosis type VI (MPS VI) is a recessive disorder, no family history is usually present.
Physical
- Facial features include the following:
-
- Coarse facial features (Compare the facial features with those of other family members to best appreciate the coarsening.)
- Macrocephaly
- Enlarged tongue
- Prominent forehead
- Possible coarse texture of hair
- Hepatomegaly and splenomegaly are often present in patients with MPS VI.
- Umbilical and inguinal hernias are common.
- Growth may be normal for several years and may then stop, resulting in a final stature of 90-140 cm. A short trunk with lumbar lordosis is typically present.
- Corneal opacities can be detected with slitlamp examination.
- Restricted joint movement, including claw-hand deformities, appears in the first few years of life.
- Examination of the skin frequently reveals hirsutism.
Causes
MPS VI results from the deficiency of N-acetylgalactosamine 4-sulfatase (arylsulfatase B) and the lysosomal accumulation of dermatan sulfate.
Mucopolysaccharidosis Type I H/S
Mucopolysaccharidosis Type IH
Mucopolysaccharidosis Type II
Mucopolysaccharidosis Type IS
Lab Studies
- Urine glycosaminoglycan analysis can be performed using various qualitative or quantitative methods. These studies are useful for establishing the likely diagnosis of MPS but do not provide a specific diagnosis, which requires enzymatic testing.
- Definitive diagnosis requires the determination of the specific lysosomal enzyme level in cultured fibroblasts or isolated leukocytes.
- Normal levels of a second sulfatase should be documented to exclude multiple sulfatase deficiencies.
Imaging Studies
- Perform skeletal survey studies to reveal dysostosis multiplex. Findings may include the following:
-
- Macrocephaly with an enlarged sella
- Acetabulum hypoplasia
- Ovoid deformities of the vertebrae
- Anterior hypoplasia of the L1 and L2 vertebral bodies
- Epiphyseal dysplasia of the proximal femur
- Evidence of kyphoscoliosis
- Echocardiography can reveal valvular heart disease, which is common. Acute infantile cardiomyopathy has also been reported in mucopolysaccharidosis type VI (MPS VI).
- MRI of the brain and spine may demonstrate hydrocephalus or provide evidence for spinal cord compression, especially in the cervical region.
- Flexion-extension radiography of the C-spine may demonstrate atlantoaxial instability and subluxation of C1 on C2.
Other Tests
- Perform an audiological evaluation because deafness and hearing loss are common in MPS.
- Perform an ophthalmologic examination to identify corneal opacities, vision change, and optic nerve abnormalities, suggesting increased intracranial pressure.
- Perform pulmonary function tests to monitor restrictive and obstructive disease and perform a sleep study to evaluate for sleep apnea.
Histologic Findings
Lysosomal engorgement in tissue biopsies is evident, as are vacuolated lymphocytes on peripheral blood smear.
Staging
Urine GAG level corrected for creatinine is a biochemical disease marker that can provide a crude estimate of disease severity and response to specific treatment (bone marrow transplantation [BMT] or enzyme replacement therapy).
Medical Care
Patients with mucopolysaccharidosis type VI (MPS VI) require ongoing medical care from a number of subspecialists. In addition, patients should receive routine pediatric care, including immunizations. US Food and Drug Administration (FDA)–approved enzyme replacement therapy with galsulfase (Naglazyme) has been shown to improve walking and stair-climbing capacity and to decrease urine GAG levels in patients with MPS VI.
- Perform ongoing evaluations for the development of valvular cardiac disease. Such evaluations include annual echocardiograms. According to the American Heart Association guidelines, patients should receive bacterial endocarditis prophylaxis before surgical or dental procedures.
- Many patients show evidence of restrictive airway disease, obstructive airway disease, or both. Conduct ongoing assessments for the development of clinically significant hypoventilation.
- Patients typically have contractures and hand deformities. A program of physical therapy may be beneficial in maintaining optimal function. Carpal tunnel syndrome may be present and asymptomatic and should be evaluated with nerve conduction on a regular basis.
- Patients who develop headache, vision change, or vomiting should be evaluated for increased intracranial pressure and hydrocephalus. Measuring intrathecal spinal fluid pressure to confirm increased intracranial pressure may be necessary.
Surgical Care
- Patients who develop clinically significant valvular heart disease may require valve replacement.
- Patients with obstructive airway disease sometimes benefit from tonsillectomy and adenoidectomy. Severe airway obstruction and hypoventilation may eventually require tracheostomy.
- Corneal transplants have been successful in restoring vision to patients with corneal clouding, although storage in the transplanted cornea may recur over time.
- Surgical decompression of the carpal tunnel to preserve median nerve function may be necessary.
- Neurosurgery may be required to place ventriculoperitoneal decompression shunts for hydrocephalus or increased intracranial pressure.
- Orthopedic surgery may be necessary to decompress the spinal cord or to stabilize the atlantoaxial junction.
- Patients often develop hip dysplasia and require hip replacement surgery
Consultations
- Refer all patients suspected of having an MPS to a medical geneticist. The geneticist is needed to provide definitive diagnosis and appropriate counseling of the family about recurrence risks.
- Refer affected patients to a cardiologist because of the risk for valvular heart disease.
- Refer affected patients to an audiologist for periodic hearing evaluations because both conductive and sensorineural hearing loss can occur.
- Ophthalmology: Obtain slitlamp and funduscopic examinations during the initial evaluation and then periodically thereafter. Corneal clouding can lead to significant visual impairment.
- Neurosurgery or orthopedics: Spinal cord compression secondary to thickening of the dura in the cervical canal has been described. Spinal cord compression results in myelopathy, which may require surgical intervention.
- A pulmonologist should evaluate the patient regularly to identify airway obstruction, hypoventilation, or sleep apnea.
Diet
No special dietary requirements exist.
Activity
- Patients with MPS VI usually have some limitations on their level of activity because of contractures and joint stiffness.
- Patients with cardiac manifestations may be limited in their activity level.
Specific therapy for mucopolysaccharidosis type VI (MPS VI) is just beginning to emerge, with recent clinical trials showing benefit from a recombinant DNA glycoprotein enzyme replacement therapy.
Drug Category: Enzyme replacement therapy
Recombinant DNA variant of N-acetylgalactosamine 4-sulfatase has been shown to improve physical capabilities of individuals with MPS VI.
| Drug Name | Galsulfase (Naglazyme) |
|---|---|
| Description | Indicated for MPS VI, which is characterized by the absence or marked reduction of N-acetylgalactosamine 4-sulfatase; provides exogenous enzyme as treatment. Recombinant DNA glycoprotein (Chinese hamster ovary cell line) variant form of polymorphic human enzyme N-acetylgalactosamine 4-sulfatase. Clinical trials showed improvement in walking and stair-climbing capacity. Most patients in the clinical trials were pediatric patients; however, children <5 y were not included. |
| Adult Dose | 1 mg/kg IV infused over at least 4 h qwk; may extend infusion up to 20 h if infusion reactions occur |
| Pediatric Dose | <5 years: Not established >5 years: Administer as in adults |
| Contraindications | None known |
| Interactions | None reported |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Nearly all patients develop antibodies to galsulfase (pretreat with antihistamine [eg, diphenhydramine] with or without antipyretics [eg, acetaminophen] 30-60 min prior to each infusion); severe infusion reactions have occurred despite pretreatment with antihistamines and antipyretics and may include angioneurotic edema, hypotension, dyspnea, bronchospasm, respiratory distress, apnea, and urticaria; common infusion-related reactions include fever, chills/rigor, headache, rash, and mild-to-moderate urticaria; nausea, vomiting, elevated blood pressure, retrosternal pain, abdominal pain, malaise, and joint pain may occur; initial infusion reactions may occur as late as week 55 of treatment; sedating antihistamines may cause sleep apnea; moderate-to-severe infusion-associated reactions can generally be managed by slowing infusion rate and providing corticosteroid pretreatment in the 24-h period before the infusion |
Further Inpatient Care
- Obstructive airway disease can result from narrowing of the trachea, enlarged tongue, and redundant tissue. Tracheostomy has been performed in some patients. Tonsillectomy and adenoidectomy are also frequently performed to relieve obstruction.
- Many patients develop carpal tunnel syndrome, which may require nerve decompression.
Further Outpatient Care
- Physical therapy to maximize joint mobility is beneficial.
In/Out Patient Meds
- Patients with cardiac disease may require pharmacological therapy to manage cardiac failure. Monitor these patients closely with a pediatric cardiologist.
Transfer
- Transfer patients with mucopolysaccharidosis type VI (MPS VI) who require general anesthesia for any procedure to a facility equipped to handle the substantial anesthetic risks.
Deterrence/Prevention
- In most cases, a history of MPS VI is not present, and the affected child is the first affected individual in the family.
- In future pregnancies, prenatal diagnosis is possible.
Complications
- Vision loss due to corneal clouding is common. Corneal transplants have been reported.
- Hearing loss is common and may require hearing aids.
- Carpal tunnel syndrome is a common complication.
- Obstructive airway disease can result in snoring or even hypoventilation.
- Valvular heart disease is common and may require surgical intervention.
Prognosis
- MPS VI is a progressive disorder with significant morbidity and early mortality. As with many genetic inborn errors of metabolism, considerable variation exists among individual patients. Therefore, the prognosis for a particular patient must be determined after consideration of the presentation and complications.
Patient Education
- Counsel patients and their families about the autosomal recessive inheritance pattern of MPS VI, the risk for occurrence in future pregnancies, and the availability of prenatal diagnosis.
Medical/Legal Pitfalls
- Failure to counsel parents of affected individuals about the risk of occurrence in future pregnancies
- Failure to offer parents prenatal diagnosis studies
- General anesthesia should be administered to patients with mucopolysaccharidosis type VI (MPS VI) only in facilities staffed with anesthesiologists familiar with the potential complications. The anesthesia risk is significant because of instability of the atlantoaxial joint. Specifically, induction of anesthesia can be difficult because of airway maintenance problems.
Special Concerns
- Anesthesia risk: MPS VI presents a significant anesthesia risk because of instability of the atlantoaxial joint. In particular, induction of anesthesia can be difficult because of problems maintaining the airway. Patients with MPS VI should undergo general anesthesia only in facilities staffed with anesthesiologists who are familiar with the potential complications.
- Experimental therapies: BMT has been attempted in a number of patients with MPS. Although BMT has been of particular interest in treating patients with MPS who are at risk for neurologic disease (MPS IH), BMT has been limited by the associated mortality risk and the need for an appropriately matched donor. Refer patients and families interested in pursuing this option to a center with staff who are experienced in this procedure for patients with metabolic disease.
