Jun 20, 2019 acidemia propionica pdf propionic acidemia is an inherited disorder in which the body is unable to process certain parts of proteins and lipids fats properly. Methylmalonic acidemia, vitamin b12 responsive the british inherited metabolic disease group bimdg has published on its website guidelines for the emergency management of patients with inherited metabolic disorders. Variable dietary management of methylmalonic acidemia. Listing a study does not mean it has been evaluated by the u. Methylmalonic acidemiaaciduria mma is a genetically heterogeneous group of inherited metabolic disorders biochemically characterized by the accumulation of methylmalonic acid. Here are the ones the management for an acute decompensation in children and adults with methylmalonic acidemia due to a. Jan 19, 2016 methylmalonic acidemia is an inherited disorder in which the body is unable to process certain proteins and lipids properly.
The effects of methylmalonic acidemia vary from mild to lifethreatening. Methylmalonic acidemia mma is an inherited organic acidemia usually present with recurrent episodes of acute illness. These advances were possible thanks to new pathophysiological insights. Methylmalonic acidemia and the disease associated with the more proximal defect in the same pathway, propionic acidemia, are the most common clinically significant genetic disorders of organic acid metabolism fenton and rosenberg 1995. Methylmalonic acidemia stems from several genotypes, all forms of the disorder usually diagnosed in the early neonatal period, presenting progressive encephalopathy, and secondary hyperammonemia. Like other mitochondrial enzymopathies, enzyme replacement therapy ert is not available, and although promising, aav gene therapy can be limited by preexisting immunity and has been associated with genotoxicity in mice. Methylmalonic acidemia controlled with oral administration. Multiple conditions canbe included in an import file. This document has been published in the federal register. Identification of a novel deletion in the mmaa gene in two. Prevalence of complications occurring in pa and mma. Glutaric acidemia type 1 type 2 hyperlysinemia pipecolic acidemia saccharopinuria. There is a 1 in 4, or 25% chance that two carriers of the gene will have a baby with methylmalonic acidemia. Carrier screening to help detect the risk of having a baby with a specific inherited disorder, such as cystic fibrosis.
For more information on this disorder, choose ketotic hyperglycinemia as your search term in the rare disease database. Metabolic phenotype of methylmalonic acidemia in mice and. Select up to three search categories and corresponding keywords using the fields to the right. Methylmalonic acidemia information mount sinai new york. Methylmalonic acidemia mma is an autosomal recessive inherited disorder that is characterized by the abnormal accumulation of methylmalonylcoa and methylmalonic acid in body fluids, which is caused by either a defect in methylmalonylcoa mutase mcm, ec 5. Manufacture and commercialization of gene therapy products for human gene therapy use to treat andor prevent methylmalonic acidemia mma. Methylmalonic acidemia methylmalonylcoa mutase deficiency propionic acidemia. Methylmalonic acidemia mma incidence was evaluated based on newborn screening in xuzhou from november 2015 to december 2017, and the clinical, biochemical and molecular characteristics of patients with mma harboring mmachc and mut mutations were summarized. The result is a buildup of a substance called methylmalonic acid in the blood. Teach physicians about oa organic acidemia association. Diagnosis of methylmalonic acidemia using machine learning. Frontiers newborn screening for methylmalonic acidemia. Mma is a group of disorders in which methymalonylcoa cannot be broken down by methylmalonylcoa mutase mut, an enzyme involved in the breakdown. Pathophysiology of lifethreatening acute metabolic decompensations amd in propionic acidemia pa and isolated methylmalonic acidemia mma is insufficiently.
Methylmalonic acid quantified in dried blood spots. Insights into the molecular mechanisms of methylmalonic acidemia using microarray technology lianshu han, shengnan wu, feng han, xuefan gu department of pediatric endocrinology and genetic metabolism, xinhua hospital, shanghai institute for pediatric research, shanghai jiaotong university school of medicine, shanghai 200092, china. Methylmalonic acidemia can occur in individuals of all races and ethnicities, with an incidence in the united states of approximately 191,000 and a calculated carrier frequency of 1 in 151. Methylmalonic acidemia diagnosis by laboratory methods ncbi.
Methylmalonic acidemia is an inherited disorder in which the body is unable to process certain proteins and fats lipids properly. Files are available under licenses specified on their description page. Methylmalonic acidemia refers to a group of inherited conditions in which the body cant breakdown certain parts of proteins and fats. Methylmalonic acidemia can be caused by an inherited deficiency of methylmalonylcoa mutase, an adenosylcobalaminrequiring enzyme that converts lmethylmalonylcoa to succinylcoa figure 975, or in the metabolic pathway that catalyzes the biosynthesis of adenosylcobalamin from vitamin b 12 figure 978 and table 972.
Jan 27, 2020 methylmalonic acidemia refers to a group of inherited conditions in which the body cant breakdown certain parts of proteins and fats. Methylmalonic acidemia mma is an organic acid disorder. Individuals with this disorder have a combination of features from two separate conditions, methylmalonic acidemia and homocystinuria. The disorder can result in death if undiagnosed or left untreated.
Pdf isolated methylmalonic acidemiaaciduria is caused by complete or partial deficiency of the enzyme methylmalonylcoa mutase mut 0. Plasma total homocysteine will be elevated in the cobalamin c, d and f deficiencies. Methylmalonic acidemia new england consortium of metabolic. Methylmalonic acidemia, cobalamin c type, presenting with. Newborn screening act sheet elevated c3 acylcarnitine. Testing for methylmalonic acidemia is often done as part of a newborn screening exam. There are few detailed consensus and guidelines on perioperative clinical characteristics of liver transplantation lt in patients with methylmalonic acidemia mma. Pubmed comprises more than 26 million citations for biomedical literature from medline, life science journals, and online books. Perspectives on methylmalonic acidemia resulting from. Clinical and laboratory study of methylmalonic acidemia. Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl coa mutase perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl coa mutase ledley, fred d. Subacute bilateral visual loss in methylmalonic acidemia. Citations may include links to fulltext content from pubmed central and publisher web sites. Patients present either shortly after birth with acute deterioration.
Genetic and genomic systems to study methylmalonic acidemia. Demographic characteristics and enzymatic and mutation information for the 29 patients studied are listed by age. Acidemia propionica pdf propionic acidemia is an inherited disorder in which the body is unable to process certain parts of proteins and lipids fats properly. Jul 11, 2018 methylmalonic acidemia mma is an autosomal recessive inherited disorder that is characterized by the abnormal accumulation of methylmalonylcoa and methylmalonic acid in body fluids, which is caused by either a defect in methylmalonylcoa mutase mcm, ec 5. Multiple conditions can be included in an import file.
Signs and symptoms of this condition usually appear in early infancy and include vomiting, dehydration, hypotonia, lethargy, and failure to thrive. The result of this condition is the inability to properly digest specific fats and proteins, which in turn leads to a buildup of a toxic level of methylmalonic acid in the blood. Guven a, cebeci n, dursun a, aktekin eh, baumgartner mr, fowler b. In 14 patients with methylmalonic acidemia we studied the correlations between clinical severity considered in terms of survival and number of acute episodes, daily tolerance to proteins. Over the last decades, advances in clinical care for patients suffering from propionic acidemia pa and isolated methylmalonic acidemia mma have resulted in improved survival. Logicbio therapeutics receives rare pediatric disease designation for lb001 for the treatment of methylmalonic acidemia. In some, the dermatitis is a manifestation of untreated disease, while in others, including methylmalonic acidemia, skin lesions have been ascribed to nutritional deficiency due to therapeutic amino acid restrictions.
It was thought that the neurologic abnormalities seen in this disease were exclusively the consequences of these acute crises. Methylmalonic acidemia with homocystinuria is an inherited disorder in which the body is unable to properly process protein building blocks amino acids, certain fats lipids, and a waxy fatlike substance called cholesterol. Methylmalonic acidemia mma is usually caused by a deficiency of the enzyme methylmalonylcoa mutase mcm, a defect in the transport or synthesis of its. Patients typically present at the age of 1 month to 1 year with neurologic manifestations, such as seizure, encephalopathy, and stroke. Methylmalonic acidemia mut information for health professionals. Leave columns that do not apply to a con dition blank. Methylmalonic acidemia an overview sciencedirect topics. Individuals affected with this disorder present with lethargy, failure to thrive, recurrent vomiting, dehydration, respiratory distress, and hypotonia in the first year of life 2. Perioperative characteristics and management of liver. Treatment is aimed at reducing the sources of the precursors. Patients are prescribed a protein restricted diet to prevent elevated levels methylmalonyl coa.
Mma presents with lethargy, acidosis, hypoglycemia hyperglycemia, ketosis, and recurrent episodes. Methylmalonic acidemia mma, an autosomal recessive metabolic disease, is a type of organic acidemia. Cobalamin c disease cblc, also known as methylmalonic aciduria with homocystinuria, is an inherited disease characterized by hypotonia, lethargy, mental retardation, seizures, vision problems, and bloodrelated problems. This app is designed to support families and children with mma on protein restricted diets. Methylmalonic and propionic acidemia mmapa are inborn errors of metabolism characterized by accumulation of propionic acid andor methylmalonic acid due to deficiency of methylmalonylcoa mutase mut or propionylcoa carboxylase pcc. Methylmalonic aciduria due to methylmalonylcoa mutase. We look forward to advancing lb001 and expect to file an investigational new drug ind application in the fourth quarter of 2019. With each pregnancy, there is the same 25% chance of having a child with methylmalonic acidemia.
Methylmalonic acidemia adult metabolic diseases clinic. Propionic acidemia is a very rare genetic form of ketotic hyperglycinemia. Federal register prospective grant of exclusive license. Serum vitamin b 12 may be elevated in the cobalamin disorders. Methylmalonic acidemia mma organic acidemia association. Erosive dermatitis resembling the skin lesions of acrodermatitis enteropathica has been described in a number of aminoacidopathies and organic acidemias. Symptoms of a decompensation event include poor feeding, vomiting, trouble breathing, and lack of energy lethargy.
Teaching about metabolic diseases in medical school and residency programs is poor. Jci insight fgf21 underlies a hormetic response to. This leads to a buildup of toxic substances and bouts of serious illness called decompensation events or metabolic crises. The value of liver transplantation for methylmalonic acidemia. Perioperative characteristics and management of liver transplantation for isolated methylmalonic acidemiathe largest experience in china. Background patients with propionic acidemia usually present in the neonatal period with lifethreatening ketoacidosis, often complicated by hyperammonemia. These conditions, at one time designated as idiopathic acidosis of infancy, often result in lifethreatening acidbase disorders. Treatment attempts with highdose intravenous steroids and coenzyme q10 combined with vitamin e were ineffective. The key finding in methylmalonic acidemia is the accumulation of methylmalonic acid in body fluids and tissues. Isolated methylmalonic acidemiaaciduria mma is a devastating metabolic disorder with poor outcomes despite current medical treatments. Get a printable copy pdf file of the complete article 969k, or click on a page image below to browse page by page. Methylmalonic acidemia mmaemia is the biochemical hallmark of a group of genetic metabolic disorders that share a common defect in the ability to convert methylmalonylcoa into succinylcoa.
Clustering of mutations in methylmalonyl coa mutase associated with mut methylmalonic acidemia. Methylmalonic aciduria is a genetically heterogeneous disorder of methylmalonate and cobalamin cbl. Methylmalonic acidemia genetics home reference nih. Two types of mma that are non responsive to vitamin b12 and caused by mutations in the mmacoa mutase mut gene are referred to as mut 0 and mut. Understanding acute metabolic decompensation in propionic. This disorder is due to either a mutant methylmalonylcoa mutase apoenzyme or impaired synthesis of adenosylcobalamin, the cofactor for this enzyme. Newborn screening disorders florida administrative register. Methylmalonic acidemia controlled with oral administration of vitamin b12. Methylmalonic acidemia mma is a genetic disorder caused by a deficiency in the methylmalonylcoa mutase mcm enzyme. It is ok to leave any of these columns blank or to not include the column in the import file.
About 1 in 20 000 babies are born with methylmalonic acidemia each year in canada. Isolated methylmalonic aciduria is found in patients with mutations in the mut gene causing partial, mut, or complete, mut0, enzyme deficiency. Newborn screening disorders year added acmg code core conditions organic acid condition fatty acid oxidation disorder amino acid disorder endo disorder hgb disorder other 1 2006 prop propionic acidemia x 2 2006 mut methylmalonic acidemia methylmalonylcoa mutase x 3 2006 cbl a,b methylmalonic acidemia cobalamin disorders x. Hence, the constellation of laboratory findings in mma is the following. During the study, 236,368 newborns were screened for mma by tandem mass. The disorder presents in the early neonatal period with poor feeding, vomiting, lethargy, and lack of muscle tone. In some families, there may be only one child with. Methylmalonic acidemia mma is an autosomal recessive metabolic disorder. Methylmalonic acidemia definition of methylmalonic acidemia. Metabolics the nutricia learning center features tools and educational resources for metabolic healthcare professionals. Dec 26, 2017 methylmalonic acidemia is an autosomal recessive disorder of amino acid metabolism, involving a defect in the conversion of methylmalonylcoenzyme a coa to succinylcoa. Propionic and methylmalonic acidemia are recessive disorders of the metabolism of thr,val, ile, met, odd chain fatty acids, and cholesterol classic presentation is with shock, acidosis and hyperammonemia, neutropenia and thrombocytopenia it is diagnosed by urine organic acids methylcitrate or methylmalonic acid, plasma amino acids. Methylmalonic acidemia mma is a rare inherited metabolic disorder caused by deficiency of the enzyme methylmalonylcoa mutase. Among mma, the cblc type were characterized megaloblastic anemia, growth disorder and neurological symptoms zhang et al.
The effects of methylmalonic acidemia, which usually appear in early infancy, vary from mild to lifethreatening. A typical episode is ushered in with ketonuria and vomiting, followed by acidosis, dehydration, and lethargy, leading, in the absence of. It is estimated that the incidence of mma in western populations ranges from 1. Methylmalonic acidemia mma, an organic acidemia characterized by metabolic instability and multiorgan complications, is most frequently caused by mutations in methylmalonylcoa mutase mut. Methylmalonic acidemia, also called methylmalonic aciduria, is an autosomal recessive metabolic disorder that disrupts normal amino acid metabolism. Get a printable copy pdf file of the complete article 1. Refer to the help section for more detailed instructions. Pathophysiology of propionic and methylmalonic acidemias. Methylmalonic acidemia is a form of ketotic hyperglycinemia. Understanding acute metabolic decompensation in propionic and. Methylmalonic acidemia with homocystinuria genetics home. Traditional diagnosis needs physicians personal level of professional medical knowledge and clinical experience. Links to pubmed are also available for selected references.
To define the metabolic adaptations in mma in acute and chronic settings, we studied a mouse model generated by transgenic expression of mut in the muscle. The patients underlying disease was metabolically well controlled by strict diet and carnitine supplementation. Methylmalonic and propionic acidemia mmapa are autosomal recessive disorders of propionate catabolism caused by defects in the enzymes methylmalonylcoa mutase mut or propionylcoa carboxylase pcc characterized by accumulation of metabolites of branchedchain amino acid catabolism such as 3hydroxypropionic acid, methylcitric acid andor methylmalonic acid in plasma. Methylmalonic acidemia mma is a group of rare approx. Methylmalonic acidemia methelmalonic acideemeea is genetic disorder that affects how protein is broken down in the body. Affected infants can experience vomiting, dehydration, weak muscle tone hypotonia, developmental. Neurologic nonmetabolic presentation of propionic acidemia. Logicbio therapeutics receives rare pediatric disease. Isolated methylmalonic acidemiaaciduria is caused by complete or partial deficiency of the enzyme methylmalonylcoa mutase mut 0 enzymatic subtype or mut. Media in category methylmalonic acidemia this category contains only the following file. Each document posted on the site includes a link to the corresponding official pdf file on govinfo. The patient presented today with methylmalonic acidemia provides us with an opportunity to discuss not only this condi. Acidemia, methylmalonic nord national organization for. Mild clinical features of isolated methylmalonic acidemia.
The united states department of health and human services recommends screening for this condition at birth because early detection and treatment is helpful. Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl coa mutase. Proposed guidelines for the diagnosis and management of. Propionic acidemia, also known as propionic aciduria or propionylcoa carboxylase deficiency pcc deficiency, is a rare autosomal recessive metabolic disorder, classified as a branchedchain organic acidemia.
Moreover, it could represent an ideal tier2 test for confirmation of methylmalonic acidemia, reducing the number of falsepositive results of routinely applied methods. It involves defects in a protein used to change vitamin b. Source and compound parameters for mma quantification by msms 1 pdf file. Generation of a human ipsc line sdqlchi021a from a. Methylmalonic acidemia mma is an autosomal recessive hereditary disease wang et al. Clustering of mutations in methylmalonyl coa mutase. Methylmalonic acidemia mimicking diabetic ketoacidosis in. This pdf file can be printed as a 2sided document print and copy all pages, including blank pages. Two types of mma that arenon responsive to vitamin b12 and caused by mutations in the mmacoa mutase mut gene are. The class of methylmalonic acidemia is assigned on the basis of the results of the 14 cpropionate incorporation assay, which indirectly measures the activity of the mut methylmalonylcoenzyme a enzyme. Methylmalonic acidemia kansas department of health. The central emergency features of the mma are profound metabolic ketoacidosis and hypoglycemia.
Methylmalonic acidemia is the biochemical hallmark of a group of autosomal recessive genetic metabolic disorders that prevent the body from converting lmethylmalonylcoa into succinylcoa. Methylmalonic acidemia is a disorder in which the body cannot break down certain proteins and fats. These disorders are caused by mutations in the methylmalonylcoa mutase apoenzyme or by impaired synthesis of the enzymatic cofactor, 5deoxyadenosylcobalamin 2, 3. Methylmalonic acidemia mimicking diabetic ketoacidosis in an infant. Mma due to mut gene mutations usually led to severe phenotype, and around 3540% of cases are due to new. The main cause of this disease is a defect in the conversion of methylmalonyl coa to succinyl coa. Original article insights into the molecular mechanisms of. Toxic damage of both optic nerves due to mma is the most likely mechanism. This page was last edited on september 2009, at 05. Isolated methylmalonic acidemia aciduria mma is a devastating metabolic disorder with poor outcomes despite current medical treatments.
Isolated mma is primarily caused by the deficiency of methylmalonylcoa mutase mma mut. Most of the patients show acute deterioration, metabolic. All structured data from the file and property namespaces is available under the creative commons cc0 license. Doctors dont usually test newborns for methylmalonic acidemia, but because it may cause the unexplained deaths and serious illnesses of some babies, many states are now thinking of including it among the many diseases for which doctors and midwives screen infants immediately after birth. Methylmalonic and propionic acidemia mmapa are inborn errors of metabolism characterized by accumulation of propionic acid andor methylmalonic acid.
1010 296 954 1409 353 1252 936 658 1041 1123 63 1505 526 282 683 877 325 976 1259 1243 296 176 354 1457 932 1486 790 1340