Literature DB >> 28166087

Genitourinary malformations: an under-recognized feature of ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome.

Zerin Hyder1, Victoria Beale, Ruth O'Connor, Jill Clayton-Smith.   

Abstract

The ectodermal dysplasia and cleft lip/palate (EEC) syndrome describes the association of ectrodactyly, ectodermal dysplasia and orofacial clefting. As with many autosomal dominant disorders, there is variability in expression and not all of these three core features are present in every individual with the condition. Moreover, there may be additional associated features, which are under-recognized. One of these is the presence of genitourinary anomalies, some of which cause significant morbidity. This report details a further two patients with EEC syndrome and genitourinary involvement, including flaccid megacystis with detrusor muscle failure, bilateral hydronephrosis and megaureter, requiring significant renal and urological involvement during their childhood. We go on to review the literature on the diagnosis and management of genitourinary malformations in EEC syndrome.

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Year:  2017        PMID: 28166087     DOI: 10.1097/MCD.0000000000000172

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN: 0962-8827            Impact factor:   0.816


  1 in total

1.  TP63-mutation as a cause of prenatal lethal multicystic dysplastic kidneys.

Authors:  Isabel Friedmann; Carla Campagnolo; Nancy Chan; Ghislain Hardy; Maha Saleh
Journal:  Mol Genet Genomic Med       Date:  2020-09-02       Impact factor: 2.183

  1 in total

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