Global Statistics

All countries
240,231,299
Confirmed
Updated on October 14, 2021 7:22 pm
All countries
215,802,873
Recovered
Updated on October 14, 2021 7:22 pm
All countries
4,893,546
Deaths
Updated on October 14, 2021 7:22 pm

Global Statistics

All countries
240,231,299
Confirmed
Updated on October 14, 2021 7:22 pm
All countries
215,802,873
Recovered
Updated on October 14, 2021 7:22 pm
All countries
4,893,546
Deaths
Updated on October 14, 2021 7:22 pm

What Is Pfeiffer Syndrome? Symptoms, Causes, and Life Expectancy

Pfeiffer syndrome facts

  • Pfeiffer syndrome is a genetic disorder
    that results in abnormalities of the skull and facial bones as well as changes
    in the fingers and toes.
  • Pfeiffer syndrome is subdivided into
    three types.

    • People with Type I Pfeiffer syndrome
      usually have a normal lifespan and typical intelligence.
    • Those with Types II
      and III Pfeiffer syndrome have more severe defects that can impair brain
      development and function.
  • There is no specific treatment for
    Pfeiffer syndrome. Treatment is directed at improving the individual’s symptoms.
  • Pfeiffer syndrome is associated with
    mutations (changes) in the FGFR genes.
  • Pfeiffer syndrome affects about 1 out
    of every 100,000 people.
  • Pfeiffer syndrome can be inherited or
    can occur due to a new mutation, or change, in the involved gene. In cases of
    severe Pfeiffer syndrome, a new mutation is typically the cause.

What is Pfeiffer syndrome?

Pfeiffer syndrome is a rare genetic disorder characterized by premature
fusion of certain skull bones (craniosynostosis) and other birth defects in the
hands and feet. The abnormality of the skull bones causes changes in the shape
of the face and head. There are three subtypes of the syndrome, with Types II and II
being the most severe.

Pfeiffer syndrome has also been referred to as acrocephalosyndactyly type V,
ACSV, craniofacial-skeletal-dermatologic syndrome, and Noack syndrome.

What causes Pfeiffer syndrome?

Pfeiffer syndrome is inherited as an autosomal dominant genetic disorder,
meaning that only a single copy of an abnormal gene is necessary to cause the
condition. The abnormal gene can be inherited from either parent or be a result
of a new mutation (change in a gene) in the affected individual. Almost all
cases of Pfeiffer syndrome type II and type III originate from new mutations
because the parents are unaffected.

  • Pfeiffer syndrome type I is associated with mutations in genes known as FGFR1
    and FGFR2.
  • Pfeiffer syndrome type II and type III are associated with mutations
    in FGFR2.
  • Older age in the father is a known risk factor for acquiring Pfeiffer
    syndrome in the offspring due to new mutations.

Genetic Disease Types

There are a number of types of genetic inheritance, for example:

  • Single gene inheritance (for example, disorders that include cystic
    fibrosis, sickle cell anemia, and Marfan syndrome)
  • Multifactor inheritance (for example, diseases like heart disease, high
    blood pressure, arthritis, cancer, and diabetes)

Read more about genetic diseases »

What are the signs and symptoms of Pfeiffer syndrome?

Signs and symptoms of Pfeiffer syndrome include:

  • Bulging eyes
  • Wide-set eyes
  • High forehead
  • Beaked nose
  • Underdevelopment of the upper jaw
  • Prominent lower jaw
  • Protrusion of the eyes
  • Hearing loss (in over 50% of those
    affected)
  • Short fingers and toes (brachydactyly)
  • Webbing or fusion between the digits
    (syndactly)
  • Dental problems
  • Wide thumbs and big toes that bend away
    from the other digits
  • Cloverleaf-shaped head (in Type II
    Pfeiffer syndrome)

People with Type I Pfeiffer syndrome typically have normal intelligence.
Types II and III of Pfeiffer syndrome are more severe. People with types II and
III of Pfeiffer syndrome usually have problems with brain development. This can
cause limitation of brain growth and developmental delays.

How common is Pfeiffer syndrome?

Pfeiffer syndrome affects around 1 out of every 100,000 people.

How is Pfeiffer syndrome diagnosed?

Pfeiffer syndrome is diagnosed by the presence of the characteristic birth
defects. If the diagnosis is uncertain, genetic testing can be done to identify
changes in the FGFR1 and/or FGFR2 genes.

Is there any treatment for Pfeiffer syndrome?

There is no treatment that can reverse Pfeiffer syndrome, but treatments are
available that address each individual’s specific symptoms. Treatments may be
needed from a variety of specialists, including surgeons, pediatricians,
otolaryngologists (ENT specialists), neurologists, or others. Reconstructive
surgeries can help overcome some of the physical defects associated with the
syndrome.

What other disorders are related to Pfeiffer syndrome?

There is a spectrum of disorders associated with changes to the FGFR genes
that results in facial defects. These conditions include Pfeiffer syndrome and
the following:

  • Apert syndrome
  • Crouzon syndrome
  • Beare-Stevenson syndrome
  • FGFR2-related isolated coronal
    synostosis
  • Jackson-Weiss syndrome
  • Crouzon syndrome with acanthosis
    nigricans (AN)
  • Muenke syndrome

What is the life expectancy of an individual with Pfeiffer syndrome?

Most people with Type I Pfeiffer syndrome have a normal life span. People
with Types II and III have severe disease and may develop complications that
shorten their life expectancy.

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