
doi: 10.1007/bf00858684
pmid: 3153032
A 7-year-old boy presented with a history of postprandial vomiting, failure to thrive, hematuria, proteinuria and decreased renal function. Electron microscopy of a renal biopsy specimen demonstrated the typical glomerular basement membrane changes associated with Alport's syndrome. Audiometry revealed a moderate bilateral high-tone sensorineural hearing loss. Bilateral anterior lenticonus and a unilateral cataract were also diagnosed. Achalasia diagnosed radiologically and confirmed by biopsy was corrected by surgery. Evaluations of the parents and three siblings were negative. The patient subsequently developed end-stage renal failure. This case report and a review of the literature suggest that achalasia may be part of Alport's syndrome in some patients.
Esophageal Achalasia, Male, Kidney Glomerulus, Humans, Nephritis, Hereditary, Child
Esophageal Achalasia, Male, Kidney Glomerulus, Humans, Nephritis, Hereditary, Child
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