Epilepsy with myoclonic-atonic seizures

C P Panayiotopoulos MD PhD (Dr. Panayiotopoulos of St. Thomas' Hospital has no relevant financial relationships to disclose.)
Jerome Engel Jr MD PhD, editor. (Dr. Engel of the David Geffen School of Medicine at the University of California, Los Angeles, has no relevant financial relationships to disclose.)
Originally released October 18, 1993; last updated November 28, 2016; expires November 28, 2019

This article includes discussion of epilepsy with myoclonic-atonic seizures, epilepsy with myoclonic-astatic seizures, Doose syndrome, centrencephalic myoclonic-astatic petit mal, myoclonic-atonic epilepsy, myoclonic-atonic epilepsy of childhood, and myoclonic-atonic petit mal of early childhood. The foregoing terms may include synonyms, similar disorders, variations in usage, and abbreviations.


Epilepsy with myoclonic-atonic seizures is a genetic generalized epilepsy that begins between the ages of 7 months and 6 years (peak age 2 to 4 years) in previously normal children. It starts with frequent and usually lengthy febrile and afebrile generalized tonic-clonic seizures. A few weeks after onset, myoclonic, atonic, myoclonic-atonic, and absence seizures usually follow. Seizures are frequent and may cause traumatic falls. Nonconvulsive status epilepticus, sometimes lasting for many hours or days, is common. Interictal EEG shows brief, generalized 2 to 4 Hz spike/polyspike-wave discharges. Ictal EEG depends on the seizure type. Myoclonic-atonic seizures manifest with discharges of irregular spike-wave or polyspike-wave complexes at a frequency of 2.5 to 3 Hz, or more. Atonia is usually concurrent with the slow wave of a single- or polyspike-wave complex. Prognosis is uncertain because of various diagnostic criteria and treatment strategies. In general, seizures remit 2 to 4 years after onset, but some cognitive impairment may occur. Treatment is usually with a combination of valproate and small doses of lamotrigine; other antiepileptic drugs such as ethosuximide and clonazepam may be used. Carbamazepine, phenytoin, and vigabatrin are amongst the contraindicated drugs. Ketogenic diet or modified Atkins diet may be therapeutic in drug-resistant cases. In this article, the author details the clinical manifestations, etiology, EEG, differential diagnosis, prognosis, and optimal management of patients with epilepsy with myoclonic-atonic seizures, also known as Doose syndrome.

Key points


• Epilepsy with myoclonic-atonic seizures (also known as Doose syndrome) is a genetically determined generalized (idiopathic) epilepsy with onset in infancy and early childhood.


• It manifests with frequent and multiple types of seizure (generalized tonic-clonic, myoclonic, atonic, and absence seizures), though myoclonic-atonic seizures with falls are the defining symptoms.


• EEG shows frequent generalized discharges of spike/polyspike-slow wave at varying frequencies of 2 to 4 Hz or higher.


• Differential diagnosis is often demanding and requires exclusion of structural epilepsies and epileptic encephalopathies that may imitate epilepsy with myoclonic-atonic seizures.


• The prognosis of seizures is usually good, but cognition may be affected.


• Early onset of treatment, mainly with a combination of valproate and small doses of lamotrigine, may prevent development of cognitive disturbances. Ketogenic diet or modified Atkins diet should be considered, and it may be therapeutic.

Historical note and terminology

Doose and colleagues introduced the concept of a specific clinical entity with myoclonic-atonic seizures being the core of the disorder, which he called “centrencephalic myoclonic astatic petit mal” (Doose 1965; Doose et al 1970). This disorder is now accepted as an epileptic syndrome by the ILAE, initially under the name “myoclonic-astatic epilepsy” (Commission 1989) and more recently termed “epilepsy with myoclonic-atonic seizures” (Berg et al 2010; Commission on Classification and Terminology of the International League Against Epilepsy 2014). It is also referred to as “Doose syndrome” (Kelley and Kossoff 2010), particularly the pure form of genetic nonstructural epilepsy with myoclonic-atonic seizures (Panayiotopoulos 2010).

The ILAE Task Force considered “epilepsy with myoclonic-astatic seizures” to be an idiopathic generalized epilepsy (Engel 2001), a view similar to that of Doose. Epilepsy with myoclonic-astatic seizures belongs to the epilepsies with primarily generalized seizures and, thus, is in line with absence epilepsies, juvenile myoclonic epilepsy, and infantile and juvenile idiopathic epilepsy with generalized tonic-clonic seizures. Like these types of epilepsy, epilepsy with myoclonic-astatic seizures is polygenically determined, with little nongenetic variability. The disease is characterized by the following criteria: genetic predisposition (high incidence of seizures and/or genetic EEG patterns in relatives); mostly normal development and no neurologic deficits before onset; primarily generalized myoclonic, astatic, or myoclonic-astatic seizures, short absences, and mostly generalized tonic-clonic seizures; no tonic seizures or tonic drop attacks during daytime (except for some rare cases with a most unfavorable course); generalized EEG patterns (spikes and waves, photosensitivity, 4 to 7 Hz rhythms); and no multifocal EEG abnormalities (but often pseudofoci) (Doose 1992). This is markedly in contrast to the previous 1989 classification in which epilepsy with myoclonic-atonic seizures was listed as a “cryptogenic/symptomatic” generalized epilepsy, in the same group of disorders as that of Lennox-Gastaut syndrome (Commission 1989).

The problem of defining epilepsy with myoclonic-atonic seizures may reflect a lack of specific diagnostic criteria and undefined boundaries of certain epileptic syndromes, particularly the epileptic encephalopathies, which may manifest with myoclonic-atonic seizures. In particular, this refers to Dravet syndrome, Lennox-Gastaut syndrome, and atypical benign partial epilepsy of childhood. Cases of benign and severe myoclonic epilepsy in infants may have been included in epilepsy with myoclonic-atonic seizures (Doose 1992; Stephani 2006). Other myoclonic epilepsies with brief seizures reported as intermediate cases between epilepsy with myoclonic-atonic seizures and Lennox-Gastaut syndrome probably prove this point (Aicardi and Levy Gomes 1992). However, it is generally accepted that some children with myoclonic-atonic seizures are otherwise normal, with no discernible causes other than a strong genetic epileptic background, and these cases probably represent the genuine, genetic syndrome of epilepsy with myoclonic-atonic seizures (or “Doose syndrome,” to distinguish them from structural epilepsies and epileptic encephalopathies with myoclonic-atonic seizures). Kaminska and colleagues presented evidence that epilepsy with myoclonic-atonic seizures is distinct from Lennox-Gastaut syndrome, and the distinction appears from the first year of the disorder (Kaminska et al 1999).

Another important point to remember is that this syndrome mainly manifests with myoclonic-atonic seizures, and these are not synonymous with myoclonic-astatic seizures.

In the 2014 ILAE “epilepsy diagnosis” manual, epilepsy with myoclonic-atonic seizures is considered a childhood epilepsy syndrome of an epileptic encephalopathy and is described as follows (Commission on Classification and Terminology of the International League Against Epilepsy 2014):


Epilepsy with myoclonic-atonic seizures (previously known as epilepsy with myoclonic astatic seizures, or Doose syndrome) is a syndrome characterized by the presence of myoclonic-atonic seizures in an otherwise normal child who may have a history of febrile and/or afebrile seizures. There is often a family history of seizures.

Clinical context: This syndrome is characterized by seizures that have onset between 6 months and 6 years of age (peak 2 to 4 years). In two thirds of children febrile seizures and generalized convulsive seizures precede the onset of myoclonic-atonic and atonic seizures. Both sexes are affected, with a male predominance (ratio 2:1). Antecedent and birth history is unremarkable. Neurological examination and head size are normal. Development and cognition is typically normal, however impairments may develop at or after seizure onset.

Caution: Glucose transporter disorders should be excluded.

Note: Epilepsy with myoclonic-atonic seizures is considered an 'epileptic encephalopathy'. This term denotes the concept that the epileptic activity itself might directly contribute additional cognitive and behavioral impairments over those expected from the underlying etiology alone, and that suppression of epileptic activity might minimize this additional impairment.

Further details of the complete description of epilepsy with myoclonic-atonic seizures can be accessed at www.epilepsydiagnosis.org.

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