Gastrocutaneous syndrome

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Editor-In-Chief: Prab R Tumpati, MD
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Gastrocutaneous syndrome
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Synonyms Gastrocutaneous fistula
Pronounce N/A
Specialty N/A
Symptoms Gastroesophageal reflux disease, abdominal pain, vomiting, diarrhea
Complications Malnutrition, dehydration, electrolyte imbalance
Onset Infancy or early childhood
Duration Chronic
Types N/A
Causes Genetic mutation
Risks Family history
Diagnosis Genetic testing, endoscopy
Differential diagnosis Peptic ulcer disease, Crohn's disease, ulcerative colitis
Prevention Genetic counseling
Treatment Nutritional support, surgical intervention
Medication Proton pump inhibitors, antacids
Prognosis Variable, depends on severity
Frequency Rare
Deaths N/A


Gastrocutaneous syndrome is a rare autosomal dominant cutaneous condition characterized by multiple lentigines.

Other names[edit]

Peptic ulcer/hiatal hernia, multiple lentigines/cafe-au-lait spots, hypertelorism, myopia

Pathophysiology[edit]

It is a rare, syndromic, hyperpigmentation of the skin characterized by multiple lentigines and café-au-lait spots associated with hiatal hernia and peptic ulcer, hypertelorism and myopia.

See also[edit]

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