Bowen–Conradi syndrome
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
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
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
Diagnosis of Bowen-Conradi syndrome is based on the presence of characteristic clinical features. Genetic testing can confirm the diagnosis.
Treatment
There is currently no cure for Bowen-Conradi syndrome. Treatment is supportive and based on the signs and symptoms present in each individual.
Prognosis
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
References
External Links
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