Mungan syndrome

Mungan Syndrome

Mungan Syndrome (pronunciation: /ˈmʌŋɡən sɪnˈdroʊm/) is a rare genetic disorder that primarily affects the urinary system and digestive system.

Etymology

The syndrome is named after Dr. Cem Mungan, a Turkish pediatrician who first described the condition in 1997.

Definition

Mungan Syndrome is characterized by congenital anomalies of the kidney and urinary tract, gastrointestinal abnormalities, and a range of other symptoms.

Symptoms

The symptoms of Mungan Syndrome can vary greatly from person to person. However, common symptoms include hydronephrosis, vesicoureteral reflux, constipation, and abdominal pain. Some individuals may also experience growth retardation and intellectual disability.

Diagnosis

Diagnosis of Mungan Syndrome is typically based on the presence of characteristic clinical signs and symptoms. Genetic testing may also be used to confirm the diagnosis.

Treatment

Treatment for Mungan Syndrome is typically supportive and based on the symptoms present in each individual. This may include surgery to correct urinary tract abnormalities, medication to manage gastrointestinal symptoms, and physical therapy to improve motor skills.

Prognosis

The prognosis for individuals with Mungan Syndrome varies depending on the severity of symptoms and the presence of other health conditions.

See Also

• Genetic disorder
• Urinary system
• Digestive system
• Congenital anomalies
• Kidney
• Urinary tract
• Gastrointestinal

External links

• Medical encyclopedia article on Mungan syndrome
• Wikipedia's article - Mungan syndrome

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