Skip to main content

Face Blindness (Prosopagnosia)


Face blindness is the colloquial term for a mental health condition, prosopagnosia. Essentially, this condition means that you cannot recognize people’s faces, although you may be able to recognize other characteristics about them, like their voice, the shirt you first met them in, or the surroundings you normally see them in, like work.

Unfortunately, this condition can deeply impact everyday life, including job prospects, friendships, and dating relationships. Tricks used to remember people do not work forever, and the interaction can then become tense, unhappy, or uncomfortable.

People with prosopagnosia may avoid social interaction because of their condition and develop social anxiety disorder. Depression is also common, and struggles with relationships and careers are also common.

Failing to recognize the faces of people you care about is one of the sadder effects of this condition, but other impacts of face blindness may not even relate to faces. These include: 

  • Failure to recognize facial expressions or emotions.
  • Struggles to understand television or movies because of an inability to recognize characters.
  • Inability to determine a person’s gender.
  • Trouble following a person’s gaze or looking in their eyes.
  • Difficulty recognizing objects or places.
  • Trouble navigating, processing angles, and understanding distance.
  • Difficulty remembering places or landmarks.

There are two types of prosopagnosia:

1.Developmental prosopagnosia is part of brain development from childhood.

2.Acquired prosopagnosia occurs if the person experiences brain damage, such as through a brain injury or a stroke.

What are the symptoms of face blindness?



The most common symptom of face blindness is an inability to recognize or discriminate between faces. This may make forming relationships more difficult, both in a personal and professional setting. It may be extremely difficult for people with face blindness to identify a person who shows up in a different setting or context than the one they’re used to.

People with minor prosopagnosia may just struggle to differentiate or identify faces of strangers or people they don’t know well. Those with moderate to severe face blindness may struggle to recognize faces of people they see regularly, including family members and close friends. In very severe faces, people with face blindness may not recognize their own faces. This may cause social anxiety or depression.

If you have prosopagnosia, you won’t forget a few faces every so often; it will be a consistent and recurring problem that doesn’t go away.

If your child has face blindness, they may:

  • wait for you to wave before they come over when you’re picking them up from school or an event
  • approach strangers thinking they’re you, or someone they know, when they’re supposed to go to a specific person
  • not recognize familiar people, like neighbors, close relatives, or family friends, especially when they see them out of context
  • become clingy or withdrawn in public places
  • have difficulty following plots of characters in movies or TV shows
  • have difficulty making friends
  • seem withdrawn at school, but confident at home

What causes face blindness?

Prosopagnosia is thought to be caused byTrusted Source abnormalities, impairment, or damage of a fold in the brain called the right fusiform gyrus. This area in the brain plays an important role in coordinating the neural systems that affect facial memory and perception.

Prosopagnosia can be caused by stroke, injury to the brain, or some neurodegenerative diseases.

In some cases, people are born with face blindness as a congenital disorder. In these cases, there seems to be a genetic link, as it runs in families.

Face blindness isn’t always a standard symptom of autism, but it seems to be more common in those with autism than in the general population. It’s theorized that face blindness may be part of what sometimes impairs the social development of people with autism.

It’s important to note that face blindness is not caused by impaired vision, learning disabilities, or memory loss. It’s a specific problem with recognizing faces as opposed to a memory problem of failing to remember the person.

How is face blindness diagnosed?

If you’re having trouble recognizing faces, your primary care physician will refer you to a neurologist.

The neurologist may have you take an assessment that evaluates your ability to recognize facial features. The assessment may evaluate your ability to:

  • recognize faces you’ve never seen, or faces of your family
  • notice differences or similarities of facial features in sets of faces shown to you
  • detect emotional cues from a set of faces
  • assess information like age or gender from a set of faces

The Benton Facial Recognition Test (BFRT) and Warrington Recognition Memory of Faces (RMF) are two tests that physicians may use to evaluate potential face blindness. The scores you get on these tests, however, may not be entirely reliable in diagnosing facial blindness outright. One study found Trusted Source that irregular scores were not actually consistent with face blindness. A physician’s opinion is much more valuable.

There are also plenty of tests that claim to be able to diagnose face blindness online. Many of these are not accurate or valid, and you’re better off consulting your physician if you’re concerned.

How is face blindness treated?

There is no cure for face blindness. Treatment focuses on helping people with the condition find coping mechanisms to better identify individuals.

You could, for example, learn to focus on other visual or verbal clues to identify a person. This could include taking note of their curly blonde hair, their shorter-than-average-height, or their voice. You may also notice certain mannerisms, like how quickly they walk.

Many researchers are working on understanding specific causes of the condition and are looking for treatment.

What causes facial blindness?

Prosopagnosia is thought to be the result of abnormalities, damage, or impairment in the right fusiform gyrus, a fold in the brain that appears to coordinate the neural systems that control facial perception and memory. Prosopagnosia can result from stroke, traumatic brain injury, or certain neurodegenerative diseases.

What are the complications of face blindness?

  • Face blindness can lead to the following complications:
  • Depression 
  • Social anxiety
  • Social withdrawal 
  • Lack of confidence 
  • Difficulty building and maintain relationships
  • Difficulty following characters in movies or TV shows.

Developmental prosopagnosia:

 In other situations, you could have the condition without any brain damage. Some data shows that there could be a genetic factor that causes developmental prosopagnosia. Many people with this type of disorder have at least one close family member with it as well.

Studies suggest that 1 in 50 people have this form. If you were born with the condition, you may not even realize that you have it.

Comments

Popular posts from this blog

Charge Syndrome

Overview CHARGE syndrome is a recognizable genetic syndrome with known pattern of features. It is an extremely complex syndrome, involving extensive medical and physical difficulties that differ from child to child. CHARGE syndrome is correlated with genetic mutation to CHD7 and the prevalence of CHARGE syndrome is 1:10,000-1:15,000 live births. Babies with CHARGE syndrome are often born with life-threatening birth defects. They spend many months in the hospital and undergo many surgeries and other treatments. Swallowing and breathing problems make life difficult even when they come home. Most have hearing two little girls sitting on a carpet, one girl has a trach and is biting her finger.loss, vision loss, and balance problems that delay their development and communication. Despite these seemingly insurmountable obstacles, children with CHARGE syndrome often far surpass their medical, physical, educational, and social expectations. One of the hidden features of CHARGE syndrome is the ...

Legg–Calve–Perthes disease

  Legg–Calve–Perthes disease Overview Legg-Calve-Perthes (LEG-kahl-VAY-PER-tuz) disease is a childhood condition that occurs when blood supply to the ball part (femoral head) of the hip joint is temporarily interrupted and the bone begins to die. This weakened bone gradually breaks apart and can lose its round shape. The body eventually restores blood supply to the ball, and the ball heals. But if the ball is no longer round after it heals, it can cause pain and stiffness. The complete process of bone death, fracture and renewal can take several years. To keep the ball part of the joint as round as possible, doctors use a variety of treatments that keep it snug in the socket portion of the joint. The socket acts as a mold for the fragmented femoral head as it heals. Symptoms Symptoms of Perthes disease include: Limping. Pain or stiffness in the hip, groin, thigh or knee. Limited range of motion of the hip joint. Pain that worsens with activity and improves with rest. Perthes diseas...

Kernicterus

  Kernicterus Overview Kernicterus is a rare condition that affects your baby’s brain when they have too much bilirubin in their blood (hyperbilirubinemia). Bilirubin is a yellow waste product that your body makes. Sometimes, your liver can’t remove enough bilirubin to keep you healthy. Too much bilirubin can cause jaundice. This is when your skin, the whites of your eyes and your gums or the area underneath your tongue (mucous membranes) appear yellow. Symptoms of kernicterus progress in stages. In addition to jaundice, symptoms usually affect newborns and include irritability, poor feeding and seizures. Complications can lead to hearing loss and permanent brain damage. If you notice changes to your newborn’s behavior or appearance, contact their healthcare provider immediately. You may hear your healthcare provider call kernicterus “bilirubin encephalopathy.” Jaundice is common in newborns. Healthcare providers will monitor newborn jaundice to decrease your baby’s risk of develop...