The international standard of care committee for congenital myopathies performed a. However, different genes have now been identified as associated with the various. The congenital myopathies are a group of rare muscle. Mar 05, 2020 congenital myopathies are caused by one or more genetic abnormalities in genes that control muscle development. Download fulltext pdf download fulltext pdf congenital myopathies. Congenital myopathies definition myopathies are diseases that cause weakness and hypotonia poor tone in the muscles that control voluntary movements. Congenital myopathies account for one of the top neuromuscular disorders in the world today, comprising approximately 6 in 100,000 live births every year.
Congenital myopathy panel the university of chicago. If this is the case, youll likely start by seeing your childs pediatrician or a primary care doctor. Pdf congenital myopathies and neonatal bone fractures. Congenital myopathies can be inherited in an autosomaldominant, autosomalrecessive, or xlinked pattern. The exams can detect problems with muscle tone and contraction, and the histories can bring to light patterns of inheritance and conditions that might have aggravated the. No specific treatment is currently available for congenital myopathies, although several specific therapies including gene therapy are either in preclinical development andor in early trials. Niall tubridy, bertrand fontaine and bruno eymard congenital myopathies and congenital myopathic dystrophies are distinct groups of inherited diseases of muscle, genetically heterogeneous, that manifest in early life or infancy. A pubmed search of all articles published in the english language with the terms congenital myopathy, nemaline myopathy, core myopathy, centronuclear myopathy, myosin storage myopathy, congenital fibertype disproportion, and pregnancy was undertaken. Congenital myopathies msd manual professional edition. The term congenital myopathy was originally used to describe a group of myopathic disorders presenting preferentially, but not exclusively, at birth and being morphologically distinct from congenital muscular dystrophies. Onset in early life with hypotonia, hyporeflexia, generalized weakness that is more often proximal than dis. Facts about myopathies muscular dystrophy association. Clinical phenotypes and new diagnostic tools article pdf available in italian journal of pediatrics 431 december 2017. Congenital muscular dystrophy congenital myopathy ullrich congenital muscular dystrophy nemaline myopathy central core myopathy centronuclear myopathy merosin deficiency congenital muscular dystrophy.
Congenital myopathies diagnosis and treatment mayo clinic. Description of arrhythmias in myopathies and muscular dystrophies is very important, because arrhythmias have a strong impact on the outcomes for these patients and are potentially treatable. Congenital myopathies are a group of genetic muscle disorders characterized clinically by hypotonia and weakness, usually from birth, and a. Congenital myopathy is a clinicopathological concept of characteristic histopathological findings on muscle biopsy in a patient with earlyonset weakness. Therefore, myopathy is a medical condition involving. Pdf approach to the diagnosis of congenital myopathies. Medline abstract for reference 2 of congenital myopathies.
This introductory chapter will provide an overview of the clinical features that alert the clinician to the likely. Congenital myopathies comprise a clinical, histopathological, and genetic heterogeneous group of rare hereditary. Care for congenital myopathies uc san diego health. Congenital muscular dystrophies cmds cmds are a group of rare muscle diseases that present at birth or soon after with hypotonia, weakness, and developmental delay, similar to the congenital myopathies. In nemaline myopathy and congenital myotubular myopathy, an inadequate oxygen supply to the body during severe bouts of respiratory weakness can lead to heart problems. Congenital myopathies and anesthesia pediatric oncall. Clinical and pathologic aspects of congenital myopathies ikuya nonaka md 4. We summarise the clinical features that are most suggestive of a congenital myopathy and discuss the major differential diagnoses. It is important that patients and families receive complete information regarding the diagnostic process and the results, including hard copies for their childs own records. Individuals may have cardiac involvement, skeletal. Clinical and pathologic aspects of congenital myopathies. Congenital myopathies cms are a separate category of muscle disorders with characteristic histopathological features and include several types. The congenital myopathies are a group of genetic muscle disorders.
Congenital myopathies cms are a group of inherited myopathies most. Patients have decreased fetal movements and breech presentation. Congenital myopathy an overview sciencedirect topics. This defect primarily affects skeletal muscle fibres and causes muscular weakness andor hypotonia.
The congenital myopathies are a group of rare muscle disorders. The congenital myopathies are a clinically and genetically heterogeneous group of congenital muscle disorders with characteristic structural abnormalities evident on muscle biopsy, visible after preparation with specific histochemical stains andor on electron microscopy. The most common congenital myopathy was central core disease followed by nemaline rod myopathy and multimini core disease. In congenital myopathies, serum ck is normal or mildly elevated and electrodiagnostic findings are nonspecific.
Weakness, pain and fatigue people with cm experience muscle weakness, pain, and fatigue. To increase the knowledge about pregnancy and delivery in women with certain muscle diseases, which is important for obstetric management and family planning of affected women. These myopathies have characteristic histopathologic abnormalities on muscle biopsy, allowing a preliminary morphologic classification. Click here to view download the congenital myopathy consensus guidelines. North kn, wang ch, clarke n, jungbluth h, vainzof m, dowling jj, amburgey k, quijanoroy s, beggs ah, sewry c, et al. Congenital myopathies are a group of myopathies, usually present from birth, that display structural changes in the skeletal muscles. The serum creatine kinase ck levels are either normal or usually mildly elevated. Congenital myopathies are a group of genetic muscle disorders characterized clinically by hypotonia and weakness, usually from birth, and a static or slowly progressive clinical course. The number of genes associated with congenital myopathies is now reportedly 20, and it is clear that additional genes are yet to be identified. The obstetric histories of patients with facioscapulohumeral fsh muscular dystrophy, limbgirdle lg muscular dystrophy, and congenital myopathies cm were retrospectively evaluated. Congenital myopathy pediatric orthopaedic society of. But, the effects of some congenital myopathies may not appear until childhood or later.
Congenital myopathy is a very broad term for any muscle disorder present at birth. They emerged as a group of disorders with the wider application of histochemistry and electron microscopy in the 1950s and 1960s. Congenital myopathies metabolic myopathies mitochondrial myopathies acquired inflammatory myopathies endocrine myopathies myopathies associated with other systemic illness druginduced myopathies toxic myopathies. Congenital myopathies refer to a heterogeneous group of genetic neuromuscular disorders characterized by earlyonset muscle weakness, hypotonia, and. Pdf congenital myopathy with fiber type disproportion. Incidence the actual incidence of congenital myopathy is unknown. Write down any signs and symptoms your child is experiencing. Congenital present at birth myopathies have a genetic basis, meaning they can be passed from parent to child. Although the clinical symptoms closely mimic each other, the genetic basis differs from disease to disease. Central core disease nemaline myopathy centronuclear myopathy. View the article pdf and any associated supplements and figures for a period of 48 hours. We report clinical and genetic characteristics of a male preterm newborn, whose phenotype was characterized by severe hypotonia and hyporeactivity, serious respiratory distress syndrome that required mechanical ventilation, clubfoot, and other dysmorphic features. Congenital myopathies are clinically and genetically a heterogeneous group of early onset neuromuscular disorders, characterized by hypotonia and muscle weakness. Then we summarise the features that are suggestive of a specific form of congenital myopathy or a specific genetic diagnosis to assist in prioritisation or interpretation of genetic testing tables 1 4.
Congenital myopathies in the adult neuromuscular clinic neurology. Congenital myopathies cm are a heterogeneous group of muscular disorders characterized by the presence of specific morphologic features on skeletal muscle biopsy, such as cores in central core disease and rods in nemaline myopathy see. Concurrent structural cardiomyopathy should be considered in patients with congenital myopathies, particularly with unexplained cardiac conduction abnormalities or contractile insufficiency. Over twenty genes have been associated with congenital myopathy subtypes. Congenital myopathic dystrophy is characterized by a dystrophic pattern, whereas no necrotic or degenerative changes. Unlimited viewing of the articlechapter pdf and any associated supplements and figures. Missense mutations of acta1 cause dominant congenital. Congenital myopathy is a term sometimes applied to hundreds of distinct neuromuscular disorders that may be present at birth, but it is usually reserved for a group of rare, inherited, primary muscle disorders that cause hypotonia and weakness at birth or during the neonatal period and, in some.
Congenital myopathies symptoms and causes mayo clinic. The evaluation of patients suspected of having a myopathy begins with a. See metabolic myopathies caused by disorders of lipid and purine metabolism and overview of inherited disorders of glucose and glycogen metabolism. View enhanced pdf access article on wiley online library html view download pdf for offline viewing.
A rare case of severe congenital ryr1associated myopathy. A muscle cell is stimulated to contract by chemical signals sent from an adjoining nerve. Nemaline myopathy, core myopathy, centronuclear myopathy. Congenital myopathy is a term sometimes applied to hundreds of distinct neuromuscular disorders that may be present at birth, but it is usually reserved for a group of rare, inherited, primary muscle disorders that cause hypotonia and weakness at birth or during the neonatal period and, in some cases, delayed motor development later in childhood. Congenital myopathies can be divided into three main clinicopathological defined categories. Congenital myopathies muscular dystrophy association. If you previously purchased this article, log in to readcube. Congenital myopathies are rare muscle diseases present at birth congenital that result from genetic defects. Congenital myopathy and cardiomyopathy with identical. Three main categories are recognized within the classical congenital myopathies. Approach to the diagnosis of congenital myopathies sciencedirect. Congenital myopathies are a clinically and genetically heterogeneous group of conditions that most commonly present at or around the time of birth with hypotonia. A decrease in glycogen, mitochondria, and ttubular system occurred in the regions showing zband abnormalities of both skeletal muscle and myocardium. Nemaline myopathy weakness is typically proximal, diffuse or selective, with or without facial weakness and the diagnostic hallmark is the presence of distinct rodlike inclusions in the.
Congenital myopathies and muscular dystrophies anatomical localisation pathological processes central nervous system deep tendon reflexes typically preserved brainsystemic disease hypoxicischaemic encephalopathy sepsis congestive cardiac failure brainstem downs syndrome praderwilli syndrome craniocervical junction congenital malformations. Congenital myopathies netherlands pdf ppt case reports. Congenital myopathy is caused by mutation of hacd1 human. In this issue of seminars in pediatric neurology, each chapter will focus on the features and management of individual congenital myopathies. There are now published guidelines for the management of children with congenital muscular dystrophies cmd and congenital myopathies cm. Symptoms of congenital myopathies some of the congenital inheritable myopathies cause severe, general muscle weakness that creates problems with basic activities like swallowing and breathing. Seminars in pediatric neurology congenital myopathies.
Other inheritable myopathies cause episodes of muscle weakness or stiffness that are milder and more localized, and temporary in nature. Congenital muscular dystrophies and congenital myopathies. Historically, congenital myopathies have been classified on the basis of major morphological features seen on muscle biopsy. Within families, there can be considerable variation with respect to disease presentation and degree of muscle involvement. The only known risk factor for congenital myopathies is having a blood relative with one of these conditions, or one or both parents who carry a mutated gene that causes them. Obstetric aspects in women with facioscapulohumeral. The term congenital myopathy was originally used to describe a group of. An overview of congenital myopathies stony brook school of. Since that time, other myopathies have been defined as congenital myopathies, which have the following characteristics.
Congenital myopathies are a heterogeneous group of disorders characterized by muscle weakness and. Mar 11, 2019 the first report of a congenital myopathy was in 1956, when a patient with central core disease ccd was described. Myomri in children with congenital myopathies is a very demanding technique with a balance between acceptable time of. Congenital present at birth myopathies have a genetic basis. This article uses a casebased approach to highlight the clinical features as well as recent advances in molecular genetics, muscle imaging, and pathophysiology of the congenital myopathies. Five forms of congenital myopathy are recognized by the international standards of care committee for congenital myopathies north et al.
Review article renaissance school of medicine at stony. There are many different types of congenital myopathies, but most share common features, including lack of muscle tone and weakness. Other signs and symptoms of some congenital myopathies include feeding and breathing difficulties, as. Mutations in megf10, a regulator of satellite cell. Pdf congenital myopathies are a heterogeneous group of.
Congenital myopathies refer to a heterogeneous group of genetic neuromuscular disorders characterized by earlyonset. Congenital myopathies can be caused by mutations in different genes, and many of the causative genes are associated with 1 histologic diagnosis. Acta1 mutations are known to cause three congenital myopathies. Congenital myopathy is a neuromuscular disorder affecting muscles under voluntary and involuntary control. Congenital myopathy cm refers to a genetically and clinically heterogeneous group of disorders characterized by muscle weakness and hypotonia at birth or in infancy. Severe congenital ryr1 associated myopathy complicated. Congenital neuromuscular disorders that severely affect diaphragmatic function are genetically heterogeneous and include nemaline and xlinked myotubular myopathies, congenital.
Advances in molecular genetics have allowed a more rational. Dastgir 2018 the most severe forms of these diseases can present in utero. Congenital myopathies are a group of rare inherited diseases, defined by hypotonia and muscle weakness. It is so named because of the metabolically inactive cores present in the muscle fibres. Congenital myopathies merck manuals professional edition. Mar 27, 2019 the national institute of neurological disorders and stroke ninds and other institutes of the national institutes of health nih conduct research related to congenital myopathies in their laboratories at the nih and also support additional research through grants to major medical institutions across the country. Others have a later onset, with symptoms appearing in childhood or adulthood. While weakness is the primary symptom, congenital myopathy can affect many different body systems and lead to additional health concerns and symptoms. There is a great clinical and genetic heterogeneity in congenital myopathies.
This disease information center provides information about three types of inherited myopathy a myopathy that can be passed from parent to child. A girl with severe congenital ryr1related myopathy exhibited atrial tachycardia and sinus node dysfunction during infancy. Congenital myopathies are rare conditions representing a wide range of disorders in muscle development and function. The inherited myopathies and muscular dystrophies are a diverse group of muscle diseases presenting with common complaints and physical signs. It is the committees goal that through these recommendations, patients with congenital myopathies will receive optimal care and improve their disease outcome. Congenital myopathy information page national institute of. Many of the congenital myopathies are due to mutations in more than one gene, and mutations in the same gene can. The congenital myopathies encompass a group of neuromuscular disorders with characteristic morphologic abnormalities in skeletal muscle, including nemaline myopathy, central core disease, multiminicore disease, and myotubular myopathy. More specifically, myopathies are diseases that cause problems with the tone and contraction of skeletal muscles muscles that control voluntary movements. Usually, diagnosis begins with evaluation of the patients personal and family history, and proceeds with physical and neurological examinations that test reflexes and strength. The term congenital means born with, but sometimes the symptoms are not immediately obvious at birth.
Congenital myopathy early onset nemaline myotubular centronuclear congenital fibretype disproportion. Central core myopathy initially presents as a floppy infant with proximal weakness. Pregnancy and delivery in women with congenital myopathies. The term congenital myopathy is applied to muscle disorders presenting in infancy with generalized muscle weakness and hypotonia followed by delayed developmental milestones. Approach to the diagnosis of congenital myopathies. Genedx believes in responsible testing that is based on established medical guidelines, and we aim to be completely transparent with our pricing so that patients, clinicians, and payers know the cost of the test. Congenital myopathies refer to a heterogeneous group of genetic. No specific treatment is available for any of the congenital myopathies, but aggressive supportive care is essential to preserve muscle activity, to allow for maximal functional ability, and to prolong life expectancy. Congenital myopathies comprise a clinical, histopathological. Congenital myopathies are a heterogeneous group of disorders.
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