What do I need to know?

  • Hemimegalencephaly is a very rare condition.

  • Most children with hemimegalencephaly have drug-resistant epilepsy.

  • Hemispheric surgery is the most common surgical treatment for hemimegalencephaly.

What is hemimegalencephaly?

Hemimegalencephaly is an extremely rare condition where one half of the brain’s cerebral cortex is larger than the other. The neurons in the enlarged half are typically malformed. Cytoarchitecture (how the neurons are stacked) is one type of deformity. It can include various types of cortical dysplasias such as polymicrogyria, pachygyria , and other brain malformations. Often, the corpus callosum is poorly formed or absent. The ventricles of the brain may be enlarged as well due to hydrocephalus .

Types of hemimegalencephaly

Isolated hemimegalencephaly: Only the cerebral cortex is involved with no associated unilateral body overgrowth, skin involvement, or systemic involvement of the organs;

Syndromic hemimegalencephaly: Not only is the brain involved, but also the skin and some organs. Conditions such as linear nevus syndrome, “cafe au lait” spots, ash leaf marks , and Hypomelanosis of Ito. Skin involvement may take months or years after birth to appear. Hemihypertrophy , where one half of the body is larger than the other, may also be present. Hemihypertrophy can be mild to severe and can sometimes a risk of tumors of the kidneys and other organs. In rare cases, syndromic hemimegalencephaly can include facial infiltrating lipomatosis, Proteus syndrome, and issues with collagen which may lead to hyperextensible joints and other challenges.

Total hemimegalencephaly: Includes enlargement of cerebellum and sometimes brain stem. Total hemimegalencpehaly can be isolated or syndromic.

In some cases, hemimegalencephaly can include malformations on the other side of the brain. Sometimes these malformations may take years to find because magnetic resonance imaging (MRI) is unable to detect the malformation until the child is older.

Cause of hemimegalencephaly

Hemimegalencephaly is caused by a spontaneous mutation which occurs on the mTOR pathway at approximately the third week of gestation. It is genetic (meaning that it involves genes) but is not hereditary. There are no reported cases of two or more children with hemimegalencephaly in one family.

There is no evidence to show that hemimegalencephaly is caused by poor maternal diet or ingestion of any substance during pregnancy.


Hemimegalencephaly is very difficult to diagnose in utero. Ultrasound imaging can only detect some, but not all, forms of brain malformations. Because it is a spectrum condition (meaning there is a broad range of presentation, from mild to severe) it can often go undetected in utero.


In most cases, hemimegalencephaly will cause the child to have seizures. Seizures can begin in very early infancy and are commonly drug-resistant. Rarely, a child may not have any seizures associated with hemimegalencephaly.

There are many different types of seizures associated with hemimegalencephaly. It is important to note here that seizures in childhood, especially if they begin in early infancy, can be catastrophic to the child’s development. Uncontrolled, they can lead to profound intellectual and developmental impairment, cause development to freeze in time, and damage the developing brain. Stopping seizures as soon as possible is imperative.

Epileptic spasms (formerly known as infantile spasms) is a particularly catastrophic form of childhood epilepsy, can often occur with hemimegalencephaly. Again, it is imperative that infantile spasms are stopped as soon as possible.

A small number of children are able to maintain relative seizure control throughout their lives, but most will have drug-resistant epilepsy that requires hemispherectomy – a type of brain surgery where one half of the cerebral cortex is removed or disconnected from the other side. Sometimes, other resection surgeries may be recommended.

Shorter time seizing prior to surgery is correlated with better developmental outcomes in infants with hemimegalencephaly.

Honda R, Kaido T, Sugai K, et al. Long-term developmental outcome after early hemispherotomy for hemimegalencephaly in infants with epileptic encephalopathy. Epilepsy Behav. 2013;29(1):30–35.


Hemimegalencephaly is a spectrum condition, meaning there is a wide range of functional outcomes that are poorly reported in research literature. Most children with hemimegalencephaly have some level of intellectual disability. Some can attain near normal intellectual development if seizures are controlled. Others may have profound intellectual and motor disabilities. All children with hemimegalencephaly have hemiparesis, a type of cerebral palsy which affects one side of the body, which may range from very mild to severe. Some may have homonymous hemianopsia, a visual impairment where half the visual field is lost. Most are able to walk and talk, but not all. Some may be tube fed while others can eat a normal diet orally. Like any spectrum condition, there are outliers at both ends of the spectrum.

It is important to note that hemimegalencephaly is not always with severe intellectual disability. Normal or near-normal development may be possible if medicine controls the seizures. These children may not need hemispherectomy or other surgeries if they are meeting developmental milestones.

Functional outcomes are closely tied to seizure control and whether the brain malformation is present on both sides of the brain. It is extremely important that the child’s neurologist is proactive in ensuring that the child has no seizures. Epilepsy surgery – most often hemispherectomy/hemispherotomy – should be considered early.

For most children with hemimegalencephaly, drug-resistance will be obvious early. It may not be necessary for the child to fail two medications – surgery should be discussed sooner for these children.

In a recent study published from our patient registry, researchers looked at 45 children who had hemispherectomy for hemimegalencephaly. They found that:

  • 68% were seizure-free after surgery;
  • 43% had average or mildly impaired cognition;
  • 26% could speak age appropriately, and
  • 21% had satisfactory reading skills.
  • A total of 55%, 43%, and 17% of children first babbled, spoke their first words, and started speaking in sentences at an age-appropriate period, respectively.
  • Children who had undergone a right hemisphere resection and those who were older at epilepsy onset were more likely to have better cognitive and language outcomes.

How young can hemispherectomy be performed?

Hemispherectomy is an extremely delicate and difficult brain surgery which should only be performed by an experience pediatric epilepsy surgeon. The youngest reported case is 41 days old; however, we know an infant as young as 10 days old has had hemispherectomy surgery for hemimegalencephaly.

Hemispherectomy for hemimegalencephaly is particularly difficult for many reasons: often the blood vessels are malformed, making them difficult to locate and cut during surgery, and can sometimes cause excessive bleeding. Also, the overall brain malformation makes surgery difficult because the familiar landmarks the surgeon uses to identify various structures are often missing. The epilepsy surgeon should not only have experience performing hemispherectomy, but should also be experienced performing hemispherectomy on infants with hemimegalencephaly.

Support Groups

The Hemimegalencephaly Family Support Network is the world’s largest support group for parents of children with hemimegalencephaly. It offers an active support platform in this closed Facebook group which includes parents from all over the world. To request acceptance into the Facebook group, you must request permission to join the group. Be sure to check your message folders on Facebook (especially the “recent”folder) as administrators will contact you to ask why you want to join the group. Grandparents, siblings, and others may join the group only with the permission of the parents of the child first.

Every two years, there is a national pediatric epilepsy surgery conference in the United States for children of families affected by epilepsy surgery. The hemimegalencephaly group usually has the most attendees at this conference, and often families of children who have not yet had hemispherectomy, or whose seizures are controlled and do not need hemispherectomy, attend this conference so that they can meet other families of children with hemimegalencephaly.


  • Parents and caregivers can connect with one of our Parent Support Navigators who has a child with hemimegalencephaly.
  • Hemimegalencephaly is an extremely rare condition. Many neurologists will be unfamiliar with the condition. The International League Against Epilepsy has excellent resources for neurologists which should be reviewed here.
  • If you need financial aid to get to an experienced epilepsy center to see if your child is a candidate for hemispheric surgery to stop or reduce the seizures caused by hemimegalencephaly, apply for our surgical evaluation travel scholarship here.


Functional cognitive and language outcomes after cerebral hemispherectomy for hemimegalencephaly

Seizure and cognitive outcomes of epilepsy surgery in infancy and early childhood

Long-term developmental outcome after early hemispherotomy for hemimegalencephaly in infants with epileptic encephalopathy

Epilepsy surgery for hemispheric syndromes in infants: hemimegalencephaly and hemispheric cortical dysplasia

Hemimegalencephaly syndrome

Total hemimegalencephaly

Epilepsy surgery in infancy

Surgery for the treatment of medically intractable infantile spasms: a cautionary case