Literature DB >> 3793512

[Familial esophageal leiomyomatosis associated with Alport's syndrome in a 9-year-old boy].

B Roussel, P Birembaut, D Gaillard, J C Puchelle, G D'Albignac, F Pennaforte, M Fandre.   

Abstract

The authors describe a family in which the mother and one son are affected by oesophageal leiomyomatosis and nephritis with haematuria. The mother also presents hypertrophy of vulva and clitoris, and her son has perceptive deafness and congenital cataract. In the medical literature only 15 cases of oesophageal leiomyomatosis in children and adolescents could be found. The association with Alport's syndrome was first described by Torres and Guarner in 1983.

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Year:  1986        PMID: 3793512

Source DB:  PubMed          Journal:  Helv Paediatr Acta        ISSN: 0018-022X


  4 in total

1.  The association of anorectal leiomyomatosis and diffuse oesophageal leiomyomatosis.

Authors:  G Azzie; A Bensoussan; L Spitz
Journal:  Pediatr Surg Int       Date:  2003-08-05       Impact factor: 1.827

Review 2.  Alport's syndrome and achalasia.

Authors:  H E Leichter; J Vargas; A H Cohen; M Ament; I B Salusky
Journal:  Pediatr Nephrol       Date:  1988-07       Impact factor: 3.714

3.  Muscular hypertrophy of the oesophagus and "Alport-like" glomerular lesions in a boy.

Authors:  E Legius; W Proesmans; B Van Damme; K Geboes; T Lerut; E Eggermont
Journal:  Eur J Pediatr       Date:  1990-06       Impact factor: 3.183

4.  Leiomyomatosis of oesophagus, congenital cataracts and hematuria. Report of a case with rectal involvement.

Authors:  M Lerone; P Dodero; G Romeo; G Martucciello; P E Caffarena; M Brisigotti; P Toma; A Taccone; M Silengo
Journal:  Pediatr Radiol       Date:  1991
  4 in total

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