Cholestasis facies

From WikiMD's WELLNESSPEDIA


Cholestasis facies
Synonyms
Pronounce N/A
Specialty N/A
Symptoms Jaundice, pruritus, dark urine, pale stools, fatigue
Complications Liver cirrhosis, liver failure, osteoporosis
Onset Varies depending on underlying cause
Duration Can be acute or chronic
Types N/A
Causes Bile duct obstruction, liver disease, genetic disorders
Risks Gallstones, alcohol abuse, hepatitis, primary biliary cholangitis
Diagnosis Blood tests, imaging studies, liver biopsy
Differential diagnosis Hepatitis, Gilbert's syndrome, Dubin-Johnson syndrome
Prevention N/A
Treatment Ursodeoxycholic acid, cholestyramine, liver transplant
Medication N/A
Prognosis Depends on underlying cause and treatment
Frequency Varies globally, more common in certain populations
Deaths N/A


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]

The primary symptom of cholestasis facies is a distinctive facial appearance, which can include:

Causes[edit]

Cholestasis facies can be caused by a variety of conditions that affect the liver's ability to produce or release bile. These can include:

Diagnosis[edit]

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:

Treatment[edit]

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]