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Erratum to “Longitudinal Observation of a Patient With Rieger Syndrome and Interstitial Deletion 4 (q25–q31.1)” [Am J Med Genet Part A 152A:977–981]

✍ Scribed by Lilia Moreira; Albert Schinzel; Alessandra Baumer; Paula Pinto; Fátima Góes; Maria de Lourdes Falcao; Ana Luiza Barbosa; Mariluce Riegel

Publisher: John Wiley and Sons
Year: 2010
Tongue: English
Weight: 137 KB
Volume: 152A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.33467

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Longitudinal observation of a patient wi

Longitudinal observation of a patient with Rieger syndrome and interstitial deletion 4 (q25–q31.1)

✍ Lilia Moreira; Albert Schinzel; Alessandra Baumer; Paula Pinto; Fátima Góes; Mar 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 238 KB 👁 2 views

## Abstract Rieger syndrome (RS; OMIM 180500) is a rare autosomal dominant disorder of morphogenesis, with ocular and systemic abnormalities and variability in phenotypic expression. Some patients with RS presented with a deletion of the band 4q25 to which the homeobox gene __PIT X2__ (former __RIE