Literature DB >> 8275567

Kaufman oculocerebrofacial syndrome: report of two new cases and further delineation.

L E Figuera1, D García-Cruz, M L Ramírez-Dueñas, V Rivera-Robles, J M Cantù.   

Abstract

Two unrelated Mexican girls, aged 14 months and 6 years respectively, with Kaufman oculocerebrofacial syndrome, are reported. Both showed psychomotor retardation, microcephaly, blepharophimosis and delayed growth as the main features; the infant also presented preauricular tags and large clitoris. Comparative analysis with previous cases reveals a heterogeneous syndrome in which the micro-brachycephaly, the mongoloid slanted eyes with different anomalies, the micrognathia and the neonatal respiratory distress are the most typical characteristics of this mental retardation syndrome.

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Year:  1993        PMID: 8275567     DOI: 10.1111/j.1399-0004.1993.tb03855.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations.

Authors:  Lina Basel-Vanagaite; Rüstem Yilmaz; Sha Tang; Miriam S Reuter; Nils Rahner; Dorothy K Grange; Megan Mortenson; Patrick Koty; Heather Feenstra; Kelly D Farwell Gonzalez; Heinrich Sticht; Nathalie Boddaert; Julie Désir; Kwame Anyane-Yeboa; Christiane Zweier; André Reis; Christian Kubisch; Tamison Jewett; Wenqi Zeng; Guntram Borck
Journal:  Hum Genet       Date:  2014-03-11       Impact factor: 4.132

2.  Loss of function of the E3 ubiquitin-protein ligase UBE3B causes Kaufman oculocerebrofacial syndrome.

Authors:  Elisabetta Flex; Andrea Ciolfi; Viviana Caputo; Valentina Fodale; Chiara Leoni; Daniela Melis; Maria Francesca Bedeschi; Laura Mazzanti; Antonio Pizzuti; Marco Tartaglia; Giuseppe Zampino
Journal:  J Med Genet       Date:  2013-05-17       Impact factor: 6.318

  2 in total

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