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Article

[Esophageal leiomyomatosis revealing an Alport syndrome].

La Revue de medecine interne - 1 Jan 2009

Abbes K, Ayadi L, Makni S, Kharrat M, Affes N, Kallel R, Gouiaa N, Ben Hmida M, Hachicha J, Beyrouti M I, Sellami Boudawara T

Abstract excerpt

Alport syndrome is a rare progressive hematuric nephropathy associated with sensorineural deafness. Leiomyomatosis associated with Alport syndrome is quite rare. We report a particular case of Alport syndrome which was diagnosed in the setting of an oesophageal leiomyomatosis. Alport syndrome and leiomyomatosis are caused by mutation of the genes encoding for the alpha chain of type IV collagen. In view of the...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18433941
DOI: 10.1016/j.revmed.2008.02.025

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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