Cholestasis facies
Cholestasis facies is a medical condition characterized by a distinctive facial appearance due to prolonged cholestasis, a condition where the flow of bile from the liver is slowed or blocked. This condition is often associated with various liver diseases and genetic disorders.
Symptoms[edit | edit source]
The primary symptom of cholestasis facies is a distinctive facial appearance, which can include:
- Jaundice (yellowing of the skin and eyes)
- Pruritus (itching)
- Dark urine
- Pale stools
- Fatigue
- Loss of appetite
Causes[edit | edit source]
Cholestasis facies can be caused by a variety of conditions that affect the liver's ability to produce or release bile. These can include:
- Liver cirrhosis
- Hepatitis
- Gallstones
- Biliary atresia
- Primary biliary cirrhosis
- Primary sclerosing cholangitis
- Certain genetic disorders, such as Alagille syndrome
Diagnosis[edit | edit source]
Diagnosis of cholestasis facies is typically based on the distinctive facial appearance, along with other symptoms of cholestasis. Additional tests may be performed to determine the underlying cause, such as:
- Blood tests
- Liver function tests
- Imaging tests, such as an ultrasound or MRI
- Liver biopsy
Treatment[edit | edit source]
Treatment for cholestasis facies focuses on addressing the underlying cause of the cholestasis. This can include:
- Medications to improve bile flow
- Medications to relieve symptoms, such as itching
- Surgery to remove gallstones or treat biliary atresia
- Liver transplant in severe cases
See also[edit | edit source]
Cholestasis facies Resources | ||
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