National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Congenital myasthenic syndrome with episodic apnea



Other Names:
CMS-EA; Myasthenic syndrome congenital associated with episodic apnea; Myasthenic syndrome, presynaptic, congenital, associated with episodic apnea; CMS-EA; Myasthenic syndrome congenital associated with episodic apnea; Myasthenic syndrome, presynaptic, congenital, associated with episodic apnea; Congenital myasthenic syndrome type 1a; CMS1A; Myasthenia familial infantile; FIM; Myasthenia gravis familial infantile 2 (formerly); FIMG2 (formerly); CMS w/episodic apnea See More
Categories:
This disease is grouped under:

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

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Medical Terms Other Names
Learn More:
HPO ID
80%-99% of people have these symptoms
Dysphagia
Poor swallowing
Swallowing difficulties
Swallowing difficulty
[ more ]
0002015
Fatigable weakness 0003473
Frontalis muscle weakness
Weakness of forehead muscle
0004661
Intermittent episodes of respiratory insufficiency due to muscle weakness 0004889
Neck muscle weakness
Floppy neck
0000467
Poor suck
Poor sucking
0002033
Proximal muscle weakness
Weakness in muscles of upper arms and upper legs
0003701
Ptosis
Drooping upper eyelid
0000508
Sudden episodic apnea 0002882
30%-79% of people have these symptoms
Apneic episodes precipitated by illness, fatigue, stress 0002872
Arthrogryposis multiplex congenita 0002804
Ataxia 0001251
Bulbar palsy 0001283
Central sleep apnea 0010536
Choking episodes 0030842
Cyanosis
Blue discoloration of the skin
0000961
Decreased fetal movement
Less than 10 fetal movements in 12 hours
0001558
Difficulty walking
Difficulty in walking
0002355
Easy fatigability 0003388
EMG: impaired neuromuscular transmission 0100285
Episodic respiratory distress
Episodic difficulty breathing
0004885
Generalized muscle weakness 0003324
Intellectual disability
Mental deficiency
Mental retardation
Mental retardation, nonspecific
Mental-retardation
[ more ]
0001249
Muscle fiber atrophy
Muscle fiber degeneration
0100295
Nasal regurgitation 0011469
Nasal speech
Nasal voice
0001611
Ophthalmoplegia
Eye muscle paralysis
0000602
Recurrent respiratory infections
Frequent respiratory infections
Multiple respiratory infections
respiratory infections, recurrent
Susceptibility to respiratory infections
[ more ]
0002205
Spinal deformities 0008443
5%-29% of people have these symptoms
Areflexia
Absent tendon reflexes
0001284
Central hypotonia 0011398
Distal amyotrophy
Distal muscle wasting
0003693
Distal lower limb muscle weakness 0009053
Dysphonia
Inability to produce voice sounds
0001618
EMG: myopathic abnormalities 0003458
High palate
Elevated palate
Increased palatal height
[ more ]
0000218
Kyphoscoliosis 0002751
Limb-girdle muscle weakness 0003325
Long face
Elongation of face
Increased height of face
Increased length of face
Vertical elongation of face
Vertical enlargement of face
Vertical overgrowth of face
[ more ]
0000276
Motor delay 0001270
Narrow jaw
Narrow lower face
Narrow lower jaw
[ more ]
0012801
Pes cavus
High-arched foot
0001761
Poor head control 0002421
Seizure 0001250
Spinal rigidity
Reduced spine movement
0003306
Stridor 0010307
Toe walking
Toe-walking
0040083
Waddling gait
'Waddling' gait
Waddling walk
[ more ]
0002515
Weak cry 0001612
1%-4% of people have these symptoms
Congenital hip dislocation
Dislocated hip since birth
0001374
Diplopia
Double vision
0000651
EEG with polyspike wave complexes 0002392
Esotropia
Inward turning cross eyed
0000565
Gastroesophageal reflux
Acid reflux
Acid reflux disease
Heartburn
[ more ]
0002020
Hyporeflexia
Decreased reflex response
Decreased reflexes
[ more ]
0001265
Joint laxity
Joint instability
Lax joints
Loose-jointedness
Loosejointedness
[ more ]
0001388
Low-set ears
Low set ears
Lowset ears
[ more ]
0000369
Microretrognathia
Small retruded chin
0000308
Motor polyneuropathy 0007178
Nystagmus
Involuntary, rapid, rhythmic eye movements
0000639
Obstructive sleep apnea 0002870
Pectus carinatum
Pigeon chest
0000768
Polyhydramnios
High levels of amniotic fluid
0001561
Respiratory arrest
Breathing cessation
0005943
Sensorineural hearing impairment 0000407
Staring gaze 0025401
Percent of people who have these symptoms is not available through HPO
Abnormality of the immune system
Immunological abnormality
0002715
Autosomal recessive inheritance 0000007
Congenital onset
Symptoms present at birth
0003577
Decreased miniature endplate potentials 0003402
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation 0003403
Generalized hypotonia due to defect at the neuromuscular junction 0003397
Ophthalmoparesis
Weakness of muscles controlling eye movement
0000597
Respiratory distress
Breathing difficulties
Difficulty breathing
[ more ]
0002098
Respiratory insufficiency due to muscle weakness
Decreased lung function due to weak breathing muscles
0002747
Strabismus
Cross-eyed
Squint
Squint eyes
[ more ]
0000486
Type 2 muscle fiber atrophy 0003554
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Last updated: 7/1/2020

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.

Patient Registry

  • A registry supports research by collecting of information about patients that share something in common, such as being diagnosed with Congenital myasthenic syndrome with episodic apnea. The type of data collected can vary from registry to registry and is based on the goals and purpose of that registry. Some registries collect contact information while others collect more detailed medical information. Learn more about registries.

    Registries for Congenital myasthenic syndrome with episodic apnea:
    Congenital Muscle Disease International Registry
     

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • The MayoClinic Web site provides further information on congenital myasthenic syndromes. Click on MayoClinic to view the information page.
  • The Muscular Dystrophy Association provides further information on congenital myasthenic syndromes. Click on Muscular Dystrophy Association to view this information page.
  • Genetics Home Reference (GHR) contains information on Congenital myasthenic syndrome with episodic apnea. This website is maintained by the National Library of Medicine.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Congenital myasthenic syndrome with episodic apnea. Click on the link to view a sample search on this topic.

Selected Full-Text Journal Articles


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