ISSN:
1432-1076
Keywords:
Alport syndrome
;
Oesophageal muscular hypertrophy
;
Leiomyomatosis
;
Glomerulonephritis
;
Autosomal dominant inheritance
Source:
Springer Online Journal Archives 1860-2000
Topics:
Medicine
Notes:
Abstract A patient with idiopathic muscular hypertrophy of the oesophagus, bilateral cataracts and an Alport-like nephropathy is described. Only 15 patients with a similar association have been described so far and autosomal dominant inheritance is most likely.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF02034748
Permalink