Literature DB >> 18955897

Trisomy 22pter-q12.3 presenting with hepatic dysfunction variability of cat-eye syndrome.

Aleksandra Jezela-Stanek1, Anna Dobrzańska, Dorota Maksym-Gasiorek, Wojciech Trzeciakowski, Anna Gutkowska, Dorota Olczak-Kowalczyk, Maria Gajdulewicz, Krystyna Spodar, Justyna Czech-Kowalska, Małgorzata Krajewska-Walasek.   

Abstract

We describe the clinical characteristics of two patients with cat-eye syndrome (CES, MIM #115470) resulting from a supernumerary marker chromosome that includes 22pter-q12.3. They both presented a constellation of features typical of CES, including coloboma, auricular malformations, heart and renal anomalies, as well as hepatic dysfunction, which led to severe effects. In one case Pierre Robin sequence was diagnosed which has not been described earlier in this trisomy. Although CES is a well known, but infrequently diagnosed disorder, we draw attention both to its clinical overlaps with other disorders and, in view of the clinical variability being identified within the 22q11 region, to the importance of careful molecular examination of proximal 22q in patients with suggestive clinical signs.

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Year:  2009        PMID: 18955897     DOI: 10.1097/MCD.0b013e328317c884

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


  1 in total

1.  A de novo sSMC(22) Characterized by High-Resolution Arrays in a Girl with Cat-Eye Syndrome without Coloboma.

Authors:  C Córdova-Fletes; M G Domínguez; A Vázquez-Cárdenas; L E Figuera; V A Neira; A Rojas-Martínez; R Ortiz-López
Journal:  Mol Syndromol       Date:  2012-08-01
  1 in total

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