Bowen–Conradi syndrome

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Bowen–Conradi syndrome
Synonyms Bowen–Conradi syndrome
Pronounce N/A
Specialty N/A
Symptoms Failure to thrive, microcephaly, micrognathia, clinodactyly, rocker-bottom feet, cryptorchidism
Complications N/A
Onset Congenital
Duration Lifelong
Types N/A
Causes Genetic mutation in the EMG1 gene
Risks Autosomal recessive inheritance, higher prevalence in Hutterite populations
Diagnosis Genetic testing, clinical evaluation
Differential diagnosis Trisomy 18, Smith–Lemli–Opitz syndrome
Prevention N/A
Treatment Supportive care
Medication N/A
Prognosis Poor, often results in early childhood death
Frequency Rare, more common in Hutterite communities
Deaths N/A


Bowen–Conradi syndrome is a rare genetic disorder that is primarily characterized by growth retardation, intellectual disability, and distinctive facial features. It is most commonly found in the Hutterite population, a group of Anabaptists who live in North America.

Symptoms and Signs[edit]

The symptoms of Bowen-Conradi syndrome typically become apparent shortly after birth. These may include:

  • Growth retardation
  • Intellectual disability
  • Distinctive facial features such as a small head (microcephaly), a prominent nose, and a small lower jaw (micrognathia)
  • Other physical abnormalities such as short stature, skeletal abnormalities, and heart defects

Causes[edit]

Bowen-Conradi syndrome is caused by mutations in the EMC1 gene. This gene provides instructions for making a protein that is involved in the normal functioning of the endoplasmic reticulum, a structure within cells that is involved in protein processing and transport.

Diagnosis[edit]

Diagnosis of Bowen-Conradi syndrome is based on the presence of characteristic clinical features. Genetic testing can confirm the diagnosis.

Treatment[edit]

There is currently no cure for Bowen-Conradi syndrome. Treatment is supportive and based on the signs and symptoms present in each individual.

Prognosis[edit]

The prognosis for individuals with Bowen-Conradi syndrome is poor. Most affected individuals do not survive past infancy due to the severe health problems associated with this condition.

See Also[edit]

References[edit]

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External Links[edit]

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