Literature DB >> 7446561

Brief clinical report: renal hypodysplasia and unilateral ovarian agenesis in the penta-X syndrome.

T Toussi, F Halal, R Lesage, F Delorme, A Bergeron.   

Abstract

We report the case of a 3-year-old penta-X female with two previously undescribed anomalies: hypoplastic kidney and absent ipsilateral ovary. The gross and histologic structure of the contralateral ovary was normal, suggesting that adults with this syndrome may be fertile.

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Year:  1980        PMID： 7446561     DOI： 10.1002/ajmg.1320060209

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  4 in total

Review 1.  A case of 49,XXXXX in which the extra X chromosomes were maternal in origin.

Authors:  Y G Cho; D S Kim; H S Lee; S C Cho; S I Choi
Journal:  J Clin Pathol       Date:  2004-09       Impact factor: 3.411

2.  Is unilateral multicystic renal dysplasia sometimes heritable, and what is the risk of recurrence?

Authors:  J Bernstein
Journal:  Pediatr Nephrol       Date:  1990-11       Impact factor: 3.714

3.  Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis.

Authors:  K Zerres; M C Völpel; H Weiss
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Report of a new case with pentasomy X and novel clinical findings.

Authors:  O Demirhan; N Tanriverdi; M B Yilmaz; S Kocaturk-Sel; N Inandiklioglu; U Luleyap; E Akbal; G Comertpay; T Tufan; O Dur
Journal:  Balkan J Med Genet       Date:  2015-12-30       Impact factor: 0.519
  4 in total

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